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Positional cranial deformities are associated with prematurity evolving during the first 2 years of life due to the malleable characteristics of the skull, the first year being the main/primary therapeutic window for intervention. The objectives were (a) to describe health characteristics, peri- and postnatal pathologies, and positional cranial deformities in infants enrolled in an early intervention program and (b) to analyze the effects of a parent education-based intervention program on positional cranial deformity in premature infants. A quantitative, analytical, longitudinal study was conducted. It included 103 premature infants enrolled in an early intervention program (EIP) during the year 2017, all under 4 months of corrected age, to whom a parent education-based intervention program was applied. Cranial circumference, cranial width, diagonals, and anteroposterior diameter were measured, and the cranial asymmetry index (CAI) and cephalic index (CI) were calculated at baseline and during two subsequent evaluations separated by a 3-month period. The main results showed that 75.7% of the infants belonged to a very premature gestational age category, and 57.3% had an adequate weight for gestational age. The most frequent pathologies were premature jaundice, premature anemia, and hyaline membrane disease. The most frequent positional cranial deformity was plagiocephaly. The parent education-based intervention program resulted in (1) a significant decrease in the CAI and a significant increase in the IC, (2) plagiocephalies: an increase in the mild category and a decrease in the moderate + severe categories, (3) brachycephalies: a decrease in the absence category and an increase in the moderate + severe category, and (4) dolichocephalies: an increase in the absence category and a decrease in the mild category. In conclusion, the recommended first line of intervention was not enough for this population, and future studies should support the development of national clinical guidelines, where education is complemented with other therapeutic measures.

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La plagiocefalia posicional (PP) es una de las causas más frecuentes de consulta en neurocirugía pediátrica. La incidencia de PP aumentó en los '90, a partir de la campaña Dormir de espaldas. Junto con el aumento de la demanda de atención, se verifica un debate acerca de la eficacia de los distintos tratamientos. La interacción padres ­ pediatra orientada a elegir la mejor terapéutica adquiere importancia, particularmente cuando se trata de decisiones sensibles a la preferencia. Es necesario saber más acerca de la naturaleza de la toma de decisiones de tratamiento de PP, para contribuir al desarrollo de procesos decisorios eficaces. Se realizó una revisión narrativa sobre investigaciones en toma de decisiones de tratamiento en PP. Se identificaron artículos en PubMed y Google Scholar (1990 ­ 2022) en una búsqueda con los descriptores "plagiocephaly", "decision making" y "parents". Se incluyeron artículos cuyo tema central fuera la toma de decisiones en PP, o que la desarrollaran como parte de otro tema. Se excluyeron trabajos en los que la toma de decisiones aparece de modo secundario o tangencial. Se encontraron 3 artículos con distintos diseños metodológicos, en los que la severidad de la presentación, los elementos socioculturales y emocionales, y los aspectos relacionados con el tratamiento son los factores más implicados en la toma de decisiones. Las relaciones entre la ansiedad parental, las expectativas de tratamiento y la percepción subjetiva de la PP, y el rol del pediatra como proveedor de información válida y confiable son temas que necesitan de ulterior investigación (AU)

Positional plagiocephaly (PP) is one of the main reasons for consultation in pediatric neurosurgery. The incidence of PP increased in the 1990s, after the "Back to Sleep" campaign. Concurrently, the growing demand for care has led to a debate regarding the effectiveness of the different treatments. The parent-pediatrician interaction is aimed at choosing the best therapeutic approach becomes important, particularly when it comes to preference-sensitive decisions. There is a need to better understand the nature of PP treatment decision-making in order to contribute to the development of effective decisionmaking processes. In this narrative review, we evaluated the research on treatment decision-making in PP. Articles were identified in PubMed and Google Scholar (1990 - 2022) using the search terms "plagiocephaly", "decision-making" and "parents". Articles were included if their central theme was decision-making in PP, or if they developed it as part of another subject. We excluded articles in which decision-making appeared in a secondary or tangential way. Three articles were identified with different methodological designs, in which the severity of the presentation, sociocultural and emotional aspects, and aspects related to treatment were the factors most implicated in decision making. The relationships between parental anxiety, treatment expectations, subjective perception of PP, and the role of the pediatrician as a provider of valuable and reliable information are topics that require further investigation (AU)

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Introducción: La tortícolis muscular congénita es una entidad clínica que se hace evidente al nacimiento o poco después, presenta un amplio espectro de secuelas; algunas de estas, una vez establecidas, pueden requerir complejas y costosas correcciones quirúrgicas. we Objetivo: Caracterizar la tortícolis muscular congénita según elementos clínicos, diagnósticos y terapéuticos. Métodos: Se realizó una búsqueda de literatura relevante sobre el tema en el primer cuatrimestre de 2021. Se utilizaron como buscadores de información científica: Pubmed/Medline, SciELO, Scopus y ScienceDirect, así como fuentes oficiales como, China CDC, CDC y FDA. La estrategia de búsqueda incluyó los siguientes términos como palabras clave: tortícolis muscular congénita, complicaciones dentofaciales y psicológicas, plagiocefalia posicional. Se evaluaron artículos de revisión, de investigación y páginas web que, en general, tenían menos de 10 años de publicados, en idioma español e inglés, y que hicieran referencia específicamente al tema de estudio a través del título. Fueron excluidos los artículos que no cumplieron con estas condiciones. Esto permitió el estudio de 90 referencias bibliográficas, de las cuales 30 se citaron en el presente artículo. Conclusiones: La tortícolis muscular congénita es una enfermedad de observancia frecuente, su diagnóstico clínico y por exámenes complementarios debe hacerse en los primeros meses de vida. La detección y tratamiento rehabilitador precoz constituyen las armas fundamentales para evitar sus secuelas dentofaciales y psicológicas.

Introduction: Congenital muscular torticollis is a clinical entity that becomes evident at birth or shortly thereafter. It presents a wide spectrum of sequelae. Some of these, once established, may require complex and costly surgical corrections. Objective: To characterize congenital muscular torticollis according to clinical, diagnostic and therapeutic elements. Methods: A search for relevant literature on the subject was carried out in the first third of 2021. As information search engines Pubmed/Medline, SciELO, Scopus and ScienceDirect were used; as well as official sources, such as China CDC, CDC and FDA. The search strategy included the following keywords: tortícolis muscular congénita [congenital muscular torticollis], complicaciones dentofaciales y psicológicas [dentofacial and psychological complications], plagiocefalia posicional [positional plagiocephaly]. Review articles, research articles and web pages, in Spanish and in English, were assessed by considering that they had generally been published within less than ten years and that they referred, within their title, specifically to the topic of study. The articles that did not meet these conditions were excluded. This allowed the study of ninety bibliographic references, thirty of which were cited in the present article. Conclusions: Congenital muscular torticollis is a frequently observed disease, which should be diagnosed, clinically and by complementary tests, in the first months of life. Early identification and rehabilitation treatment are the fundamental weapons to avoid its dentofacial and psychological sequelae.

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Introducción. La plagiocefalia no sinostósica es una condición de salud caracterizada por una asimetría de cráneo que tiene diversas consecuencias en el desarrollo. Los principales tratamientos son la kinesioterapia y el casco de moldeado craneal (CMC). Objetivo. Evidenciar la influencia de la kinesioterapia temprana en la necesidad de usar casco modelador craneal. Métodos. Se realizó un estudio cuantitativo, descriptivo y retrospectivo en lactantes mayores de tres meses ingresados al Centro de Rehabilitación Integral de Carabineros (CRICAR) con diagnóstico confirmado de plagiocefalia mediante la técnica de craneometría. Se recopilaron datos de 39 pacientes diagnosticados con plagiocefalia, evaluados y tratados entre 2017 y 2019. Se dividieron en dos grupos, ingreso temprano (bajo los 5,5 meses de edad cronológica) e ingreso tardío (sobre los 5,5 meses de edad cronológica). Resultados. Al realizar un análisis bivariado, se obtuvo que 9 de 20 pacientes tuvieron que usar CMC en el grupo de ingreso tardío, y solo 4 de 19 pacientes en el grupo de ingreso temprano. Al contrastar la razón de riesgo de usar CMC en el grupo expuesto versus el grupo no expuesto se obtiene que es 3 veces mayor, sin embargo, esta diferencia no es estadísticamente significativa (OR=3.06, IC95% 0.6-16.8) Conclusiones. El principal resultado de este estudio es la disminución en la diferencia de diagonales evaluadas con craneometría. Además, se ha observado que en nuestra muestra el uso de CMC es tres veces mayor cuando el ingreso a terapia kinesiológica es tardío.

Introduction. Non-synostotic plagiocephaly is health condition characterized by a skull asymmetry that has various developmental consequences. The main treatments are kinesiotherapy and cranial molding helmet (CMH). The purpose of this study is to evidence the influence of early kinesiotherapy on the need to use CMH. Methods. A quantitative, descriptive and retrospective study of infants older than three months, admitted to the Carabineros Comprehensive Rehabilitation Center (CRICAR) since January 2017 with a confirmed diagnosis of plagiocephaly by craniometry technique was performed. Data were collected from 39 patients diagnosed with plagiocephaly, evaluated and treated between 2017 and 2019. They were divided into two groups, early admission (under 5.5 months of chronological age) and late admission (over 5.5 months of chronological age). Results. When performing a bivariate analysis, we obtained that 9 out of 20 patients had to use CMC in the late admission group, and only 4 out of 19 patients had to use it in the opposite group. When contrasting the oods ratio of using CMC in the exposed group versus the non-exposed group we obtain that it is 3 times higher, however, this difference is not statistically significant (OR=3.06, IC95% 0.6-16.8). Conclusions. The main result of this study is the decrease in the difference in diagonals assessed with craniometry. In addition, it has been observed that in our sample the use of CMC is three times higher when admission to physical therapy is late.

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Craniosynostosis is the premature, abnormal, and non-physiological fusion of one or more cranial sutures. Its etiology can be multifactorial and genetic factors, bone abnormalities or environmental factors may be involved. Among the different types of craniosynostosis we can find anterior plagiocephaly, which generally corresponds to a non-syndromic craniosynostosis and which can affect the patient in a physiological and aesthetic way. Hemi-coronal sutures are affected in this condition. The treatment will depend on each case, although many times it is usually the surgical choice in order to prevent functional deterioration and improve the facial and cranial appearance... (AU)

La craneosinostosis es la fusión prematura, anormal y no fisiológica de una o más suturas craneales. Su etiología puede ser multifactorial y pueden estar involucrados factores genéticos, anormalidades propias del hueso o factores ambientales. Dentro de los diferentes tipos de craneosinostosis podemos encontrar a la plagiocefalia anterior, que corresponde generalmente a una craneosinostosis no sindrómica y que cual puede afectar de manera fisiológica y estética al paciente. Las suturas hemi-coronales se ven afectadas en dicha condición. El tratamiento dependerá de cada caso, aunque muchas de las veces suele ser de elección quirúrgica con el fin de prevenir el deterioro funcional y mejorar el aspecto facial y craneal... (AU)

Craniossinostose é a fusão prematura, anormal e não fisiológica de uma ou mais suturas cranianas. Sua etiologia pode ser multifatorial e fatores genéticos, anormalidades ósseas ou fatores ambientais podem estar envolvidos. Entre os diferentes tipos de craniossinostose podemos encontrar a plagiocefalia anterior, que geralmente corresponde a uma craniossinostose não sindrômica e que pode afetar o paciente de forma fisiológica e estética. Suturas hemicoronais são afetadas nessa condição. O tratamento dependerá de cada caso, embora muitas vezes seja a escolha cirúrgica para prevenir deterioração funcional e melhorar o aspecto facial e cranial... (AU)

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La craneosinostosis se define como el cierre prematuro de una o más suturas del cráneo, que se manifiesta por una forma anormal de la cabeza. Es una condición infrecuente, pero requiere ser reconocida y derivada oportunamente a Neurocirugía para prevenir complicaciones. El objetivo de esta revisión es describir las características clínicas y genéticas más frecuentes de esta patología, su clasificación de acuerdo a la forma del cráneo y los signos más característicos para lograr reconocerla oportunamente. Se realizó una búsqueda de artículos científicos en bases de datos Pubmed, Scielo y EMBASE con las palabras craneosinostosis, plagio, escafo y braquicefalia. Se seleccionaron artículos en español e inglés que describieran las características de la patología y su manejo, optando por revisiones sistemáticas o recomendaciones de sociedades científicas cuando estuvieran disponibles. La craneosinostosis puede presentarse en forma aislada o asociada a otras deformidades. Su clasifi cación depende de la(s) sutura(s) afectada(s), lo que lleva a la forma característica del cráneo y de la presencia de otras malformaciones. Suele diagnosticarse y derivarse de forma tardía, lo que se asocia a complicaciones como hipertensión endocraneana y alteración del desarrollo encefálico. La cirugía precoz tiene menor comorbilidad y mejores resultados estético. En conclusión, la forma anormal del cráneo debe hacer sospechar la presencia de craneosinostosis, aunque se presente en forma aislada. El manejo quirúrgico antes del año de vida se asocia a mejor pronóstico.

Craniosynostosis is defined as the premature fusion of one or more skull sutures, characterized by an abnormal shape of the head. It is a rare condition but should be recognized and timely referred to Neurosurgery in order to prevent complications. The objective of this review is to describe the most frequent clinical and genetic characteristics of this pathology, its classification according to the shape of the skull, and the most characteristic signs to achieve timely recognition. A search for scientific articles in Pubmed, Scielo, and EMBASE databases was performed using the terms craniosynostosis, plagiocephaly, scaphocephaly, and brachycephaly. We selected articles in Spanish and English that described the characteristics of the pathology and about its management, choosing systematic reviews or recommendations from scientific societies when available. Craniosynostosis may occur in isola tion or associated with other deformities. Its classification depends on the affected suture(s), leading to the characteristic shape of the skull and the presence of other malformations. This condition is usually diagnosed and referred late, which is associated with complications such as intracranial hy pertension and impaired brain development. Early surgery has less comorbidity and better esthetic results. In conclusion, the abnormal shape of the skull must raise the suspicion of craniosynostosis, even if it occurs in isolation. Surgical management before one year of life is associated with a better prognosis.

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PURPOSE: The current assessment of patients with craniofacial asymmetries is accomplished by physical examination, anamnesis and radiological imaging. We propose a semi-automated, computer-assisted craniofacial evaluation (SymMetric v 1.0) based on orthogonal photography of the patient's head in 3 positions. The system is simple, low-cost, no-radiation or special resources needed. Although it does not substitute CT in cases of doubt between craniosynostosis and positional plagiocephaly, multiple numeric evaluations indicate regional deformities and severity of the asymmetry, which can help in the clinical decision of indicating or not the orthosis in positional deformities, determining treatment duration or evaluating surgical outcomes after correction. METHODS: A Matlab-based tool was developed for digital processing of photographs taken in 3 positions (anterior, superior and lateral). The software guides the user to select visible and reproducible landmarks in each photograph acquisition and calculates multiple indexes and metrics, generating a set of comprehensive plots to offer the user an overview of head and facial symmetry across the orthogonal views. For purposes of demonstration, we evaluated 2 patients (one control and one with non-sinostotic deformity). RESULTS: The results show a clear differentiation of the control and plagiocephalic patient metrics mainly in the superior view, showing potential for diagnosis of the condition, and also detected the clinical improvement during helmet treatment in the follow-up, 3 and 5 months after orthosis' use. CONCLUSION: We presented a proof-of-concept for a low cost, no radiation evaluation system for craniofacial asymmetries, that can be useful in a clinical context for diagnosis and follow-up of patients.

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In the last decades alterations in the skull shape have increased at the expense of plagiocephaly, as consequence of the American Academy of Pediatrics recommendations to sleep the infant in the supine position. The clinician must differentiate between positional plagiocephaly and craniosynostosis, since if a cranial synostosis is proven, the therapeutic behavior will be potentially neurosurgical. Although three-dimensional skull tomography with bone window is the study of greater sensitivity and diagnostic specificity, the majority of cases can be confirmed by the clinic, reserving the radiography or ultrasound with a suture approach for doubtful cases. Craniosynostosis must be early referral to a craniofacial team to define the indication, opportunity and most appropriate surgical technique, in order to avoid future neurocognitive and psychosocial complications. Children with positional plagiocephaly regardless of the treatment of cranial deformity may have a higher risk of motor development delay. For correction, repositioning and physiotherapy are suggested in mild to moderate forms, reserving the use of cranial orthesis in severe forms.

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Las alteraciones de la forma del cráneo han aumentado en las últimas décadas a expensas de las plagiocefalias, como consecuencia de las recomendaciones de la Academia Americana de Pediatría de dormir al lactante en decúbito supino. El clínico debe diferenciar entre plagiocefalia posicional y craneosinostosis, ya que la conducta terapéutica será potencialmente neuroquirúrgica de comprobar una sinostosis craneal. Si bien la tomografía de cráneo tridimensional con ventana ósea es el estudio de mayor sensibilidad y especificidad diagnóstica, la mayoría de los casos pueden confirmarse por la clínica, reservando la radiografía simple o de preferencia la ecografía con enfoque de suturas para casos dudosos. Las craneosinostosis deben derivarse tempranamente a un equipo craneofacial para definir la indicación, oportunidad y técnica quirúrgica más adecuada para evitar futuras complicaciones neurocognitivos y psicosociales. Los niños con plagiocefalias posicionales, independientemente del tratamiento de la deformidad craneal, pueden tener más riesgo de retraso del desarrollo motor. Para su corrección se sugiere reposicionamiento y fisioterapia en formas leves a moderadas, reservando el uso de ortésis craneal en formas graves.

In the last decades alterations in the skull shape have increased at the expense of plagiocephaly, as consequence of the American Academy of Pediatrics recommendations to sleep the infant in the supine position. The clinician must differentiate between positional plagiocephaly and craniosynostosis, since if a cranial synostosis is proven, the therapeutic behavior will be potentially neurosurgical. Although three-dimensional skull tomography with bone window is the study of greater sensitivity and diagnostic specificity, the majority of cases can be confirmed by the clinic, reserving the radiography or ultrasound with a suture approach for doubtful cases. Craniosynostosis must be early referral to a craniofacial team to define the indication, opportunity and most appropriate surgical technique, in order to avoid future neurocognitive and psychosocial complications. Children with positional plagiocephaly regardless of the treatment of cranial deformity may have a higher risk of motor development delay. For correction, repositioning and physiotherapy are suggested in mild to moderate forms, reserving the use of cranial orthesis in severe forms.

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BACKGROUND: Many infants with congenital muscular torticollis (CMT) have deformational plagiocephaly (DP), and a small cohort also demonstrate mandibular asymmetry (MA). The aim of this retrospective study was to evaluate mandibular changes in these infants with previous computed tomography (CT) scans who underwent physical therapy (PT) to treat CMT. METHODS: A retrospective study included patients presenting to a pediatric plastic surgery clinic from December 2010 to June 2012 with CMT, DP, and MA. A small subset of these patients initially received a 3D CT scan due to concern for craniosynostosis. An even smaller subset of these patients subsequently received a second 3D CT scan to evaluate for late-onset craniosynostosis. Patients were treated with PT for at least 4 months for CMT. Initial CT scans were retrospectively compared to subsequent CT scans to determine ramal height asymmetry changes. Clinical documentation was reviewed for evidence of MA changes, CMT improvement, and duration of PT. RESULTS: Ten patients met inclusion criteria. Ramal height ratio (affected/unaffected) on initial CT was 0.87, which significantly improved on subsequent CT to 0.93 ( P < .05). None of the patients were diagnosed with craniosynostosis on initial CT. One patient was diagnosed with late-onset coronal craniosynostosis on subsequent CT. CONCLUSIONS: We identified a small cohort of infants with MA, CMT, and DP. These patients uniformly demonstrated decreased ramal height ipsilateral to the affected sternocleidomastoid muscle. Ramal asymmetry measured by ramal height ratios improved in all infants undergoing PT.

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In this retrospective cohort study, we assessed the incidence of torticollis in infants with a history of neonatal abstinence syndrome. Understanding the elevated risk of torticollis in this population is important for early identification and treatment.

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RESUMEN OBJETIVO: Revisar la fisiopatología de las craneosinostosis y las deformidades posicionales del cráneo y analizar los tipos de tratamiento, especialmente las ortesis de moldeamiento craneal. MÉTODOS: Revisión de la literatura de estudios observacionales, ensayos clínicos y de revisión en la base de datos PubMed desde 1980 a 2018 y manual de los artículos no referenciados. Se utilizaron las palabras clave: craniosynostosis, plagiocephaly, nonsynostotic, skull, cranial, asociadas a: surgical treatment, pathophysiology, cognition, orthotic devices, head protective devices. El título y el resumen fueron analizados antes de solicitar el artículo completo. En el caso de que fueran ambiguos, se analizaron los artículos en su totalidad para determinar su pertinencia. RESULTADOS: El tratamiento de las craneosinostosis es quirúrgico, mediante reconstrucción craneal, pero existe controversia respecto al manejo de deformidades posicionales: cambios de posición supervisados u ortesis de moldeamiento craneal. Aunque la corrección del defecto estético es recomendación principal de las ortesis, se discute la influencia que puede haber sobre el desarrollo cognitivo y motor, trastornos visuales, hipertensión endocraneana y defectos ortognáticos. No existen diferencias con el manejo de cambios de posición supervisada en la modificación del índice craneal. Algunos pacientes mejoran espontáneamente cuando adquieren el sostén cefálico y empiezan a incorporarse. Existen además complicaciones con las ortesis que pueden llegar a ser serias. CONCLUSIÓN: No se recomienda la utilización de medidas restrictivas como las ortesis de moldeamiento craneal para el tratamiento de estos pacientes con deformidades posicionales craneanas. La cirugía reconstructiva es el manejo de elección para las craneosinostosis.

SUMMARY OBJECTIVE: to review the pathophysiology of craniosynostosis and positional deformities of the skull, and analyze the types of treatment, especially cranial orthoses. METHODS: Review of the literature on observational studies, clinical trials and reviews in the PubMed database from 1980 to 2018 and manual search of non-referenced articles. The following keywords were used: craniosynostosis, plagiocephaly, nonsynostotic, skull, cranial, associated with: surgical treatment, pathophysio-logy, cognition, orthotic devices, head protective devices. We analyzed the title and abstract before requesting the full article. If they were ambiguous, we analyzed the whole article to determine its relevance. RESULTS: Treatment of craniosynostosis is surgical by cranial reconstruction. On the other hand, there is controversy over supervised position changes and use of cranial orthosis to manage positional deformities. Although correcting the esthetic defect is the main purpose of orthoses, their potential influence on cognitive and motor development, visual disorders, endocranial hypertension and orthognathic defects is discussed. There are no differences between conservative management with changes of supervised position and orthoses, in the modification of the cranial index. In addition, some patients improve spontaneously when they acquire cephalic support and begin to incorporate. On the other hand, there are complications with orthoses that can become serious. CONCLUSION: There is no recommendation for the use of restrictive measures such as cranial orthotics devices to treat patients with cranial positional deformities. reconstructive surgery is the treatment of choice for craniosynostosis.

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OBJECTIVE: To assess the impact of age at referral on treatment options in craniosynostosis and to identify risk factors for referral delays in this population. STUDY DESIGN: A retrospective cohort study was performed on patients with an abnormal head shape diagnosis treated at a single academic medical center between January 1, 2004 and January 1, 2014. Newly diagnosed patients with craniosynostosis were identified and referral patterns were examined. A multivariate logistic regression model was used to identify risk factors associated with the range of ages at initial referral. RESULTS: A total of 477 patients were evaluated at our institution, 197 of whom were subsequently diagnosed with craniosynostosis. The median age at initial appointment was 5.6 months (mean 8.2 months). Only 28% of children were referred within 3 months of birth. Patients referred within 3 months of birth were less likely to have had preappointment imaging than those patients referred slightly later (OR 2.53, CI 1.07-5.98, P = .035). Several variables were associated with referral after 12 months of age including multiple suture involvement (OR 4.21, CI 1.06-16.68, P = .041), minority race (OR 4.96, CI 1.91-12.9, P ≤ .0001), and referral by a nonpediatrician (OR 6.9, CI 1.73-27.49, P = .006). CONCLUSIONS: Obtaining imaging before referral to a specialist for abnormal head shape was associated with a delay in evaluation and potentially increases radiation exposure and limits treatment options in patients with craniosynostosis. In addition, children from minority groups, children referred from someone other than a pediatrician's office, and those with multiple suture craniosynostosis are at increased risk of delayed referral. Further studies into the cause of these delays are warranted.

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BACKGROUND: Osteogenesis imperfecta is an inherited disorder of the connective tissue characterized primarily by fractures with no or small causal antecedents and extremely variable clinical presentation. The disorder requires a global and, therefore, multidisciplinary therapeutic approach that should aim, among other aspects, at the prevention and treatment of deformities resulting from osteogenesis imperfecta. Due to limitations related to bony deformities, it can be difficult to place these infants in a variety of positions that would help remediate skull deformities, so a cranial orthosis becomes the therapy of choice. The aim of this study was to demonstrate the results obtained during treatment with a cranial remolding orthosis (helmet) in babies with osteogenesis imperfecta. Case Description and Methods: For the first time in the scientific literature, this study describes the use of a cranial orthosis for the treatment of infants with osteogenesis imperfecta. Both children had severe asymmetrical brachycephaly documented by laser digital scanning and were submitted to treatment with a cranial remolding orthosis. Outcomes and Conclusion: The study showed that there was a significant improvement in cranial proportion and symmetry, with a reduction in the cephalic index at reevaluation. It is concluded that the orthotic therapy is an effective therapeutic modality to improve the proportion and minimize the asymmetry in children with osteogenesis imperfecta. Clinical relevance The clinical relevance of such a description is that children with osteogenesis imperfecta may have numerous deformities and minimizing them can be an important factor. This report showed a beneficial result as the orthotic therapy modality improved the proportions and minimized the asymmetry. This treatment offers too high levels of satisfaction to parents and brings these children closer to normal indices.

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La plagiocefalia se define como el cierre prematuro de la sutura frontoparietal o coronal unilateral, la cual es causada por una sinostosis frontoparietal (unicoronal) y/o fusiones a lo largo de la sutura coronal, se caracteriza por asimetría facial en la región frontal, inclinación de la cabeza hacia el lado afectado y desviación del mentón hacia el lado no afectado. Se presenta el caso de un infante de género femenino de cinco meses de edad con plagiocefalia, asimetría facial de predominio derecho, el reborde supraorbitario y ceja están desplazados posterior y superior, tratado mediante avance frontoorbitario ipsilateral, llevado a cabo en el Hospital Regional <

Plagiocephaly can be defined as the premature closing of the frontal-parietal suture or unilateral coronal suture which is caused by a frontal-parietal (unicoronal) synostosis, and/or fusions along the coronal suture. Plagiocephaly is characterized by facial asymmetry in the frontal region, inclination of the head towards the affected side as well as deviation of the chin towards the non-affected side. We herein present the case of a five month old female infant with plagiocephaly, facial asymmetry with right side predominance, posterior and superior displacement of the eyebrow and supra-orbital ridge. The case was treated with ipsilateral frontal-orbital advancement, at the Regional Hospital <

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O número de deformidades cranianas tem aumentado desde que tiveram início os esforços internacionais dos pediatras, com a recomendação de se colocar os filhos para dormirem na posição supina, como estratégia para reduzir a morte súbita do recém-nascido. Se, por um lado, esse programa conseguiu demonstrar resultados muito eficientes nessa redução, por outro, tal recomendação fez com que os casos de assimetrias cranianas aumentassem em incidência. Isso porque os lactentes são mantidos por muito tempo em um só posicionamento, pois há também o uso abusivo de dispositivos como carrinho, bebê-conforto, cadeirinha de carro, balancinho, entre outros. Entre as assimetrias resultantes, as mais encontradas são a plagiocefalia (o crânio em forma de um paralelograma com achatamento occipital e anterior contralateral) e a braquicefalia (o achatamento occipital bilateral). Esse estudo relatou o caso de paciente com uma braquicefalia associada à plagiocefalia deformacionais tratado com órtese craniana. O paciente foi avaliado antes e após o tratamento clinicamente pelo mesmo médico, por meio de registro fotográfico e de um escaneamento a laser, que permite aferir variáveis determinantes das assimetrias. Foi possível, durante o período de tratamento, observar que houve importante melhora na simetria craniana documentada pela diminuição do índice cefálico, diminuição da diferença diagonal e ganho de volume no quadrante que se encontrava mais achatado. Conclui-se que a terapia ortótica constitui modalidade terapêutica segura e eficaz disponível para o tratamento das assimetrias cranianas posicionais.

The number of cranial deformities has increased considerably since international efforts of pediatricians to recommend parents putting their babies to sleep in the supine position as a strategy to reduce sudden death syndrome of the newborn. On the one hand, this program has demonstrated very efficient results at reducing deaths and, on the other hand, such recommendation has increased the incidence of cranial asymmetries. In addition, infants are kept too long in one position, much of this due to abusive use of strollers, baby carriers, car seats, swings and other devices. Among resulting asymmetries, the most frequently found are plagiocephaly (parallelogram shaped skull, with posterior unilateral flattening with the opposite frontal area also flattened) and brachycephaly (occipital bilateral flattening). The present study is a case report of a patient with brachycephaly associated with deformational plagiocephaly treated with cranial orthosis. The same physician clinically evaluated the patient before and after treatment using photographic recording and a laser scanning device, which allows the accurate measurement of variables determining asymmetries. It became clear during treatment that there was significant improvement in cranial symmetry documented by decrease in the cephalic index, diagonal difference and volume gain in the quadrant that was flattened. The authors conclude that orthotic therapy is a safe and effective therapeutic modality for position cranial asymmetries.

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INTRODUÇÃO: A craniossinostose coronal unilateral (CCU) é a ossificação prematura da sutura coronal unilateralmente e provoca uma deformidade em 3 dimensões, que pode afetar o crânio e as órbitas. O objetivo do presente trabalho foi aferir e comparar a assimetria do crânio e face dos pacientes portadores de CCU no período pré e pós-operatório. MÉTODO: Nove pacientes foram submetidos à correção da craniossinostose coronal unilateral, entre janeiro de 2007 a dezembro de 2010. Quatro pacientes foram do sexo feminino e cinco do sexo masculino. Foram aferidas medidas da região craniofacial para quantificar o índice de assimetria craniofacial no período pré-operatório e compará-lo com o período pós-operatório. O índice de assimetria craniofacial (IAC) foi determinado pela diferença entre as medidas craniofaciais diagonais obtidas com o goniômetro. RESULTADOS: A idade média dos pacientes submetidos à correção de CCU foi de 2 anos e 1 mês. O tempo médio de cirurgia foi de 2 horas e 46 minutos. O volume médio de sangue transfundido foi de 280 ml. A média das diferenças das medidas diagonais obtidas com o goniômetro no período pré-operatório (IAC) foi de 1,045 e do pós-operatório de 1,009 (p=0,0109), indicando forte tendência à simetria craniofacial após o ato cirúrgico. CONCLUSÃO: O tratamento proposto para as CCU foi eficiente na obtenção de simetria craniofacial. Foi necessária a sobrecorreção das estruturas ósseas para obtenção de simetria óssea no período pós-operatório.

INTRODUCTION: Unilateral coronal synostosis (UCS) is a premature fusion of the coronal suture and leads to a three-dimensional deformity that affects the cranium and orbits. The aim of this study was to compare craniofacial skeleton asymmetry preoperatively and postoperatively. METHODS: This is a retrospective study with nine patients who underwent treatment of unilateral coronal synostosis, between January 2007 and December 2010. Four patients were female and five male. The craniofacial measurements were done to quantify an index of craniofacial asymmetry preoperatively and compare to those obtained postoperatively. The craniofacial index (CI) was obtained by calculating the difference between the higher oblique measurement of the craniofacial skeleton and lower oblique measurement of the craniofacial skeleton. RESULTS: The average age of the patients who had undergone to unilateral coronal synostosis correction was 2 years and 1 month. The average time of surgery was 2 hours and 46 minutes. The blood volume transfused was 280 cc. The CI preoperatively was 1.045 and postoperatively was 1.009 (p=0.0109), indicating a tendency to craniofacial symmetry. CONCLUSION: The treatment of UCS was efficient. Bone over correction was necessary to achieve its goal of symmetry in the postoperative period.

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OBJECTIVE: The aim of this study was to perform a detailed tomographic analysis of the skull base, craniocervical junction, and the entire spine in seven patients with spondylocostal dysostosis syndrome. METHOD: Detailed scanning images have been organized in accordance with the most prominent clinical pathology. The reasons behind plagiocephaly, torticollis, short immobile neck, scoliosis and rigid back have been detected. Radiographic documentation was insufficient modality. RESULTS: Detailed computed tomography scans provided excellent delineation of the osseous abnormality pattern in our patients. CONCLUSION: This article throws light on the most serious osseous manifestations of spondylocostal dysostosissyndrome.

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Este artículo presenta el desarrollo de un prototipo de dispositivo ortésico para cráneo de pacientes con plagiocefalia occipital posicional, con el fin de aplicarlo en la rehabilitación de infantes entre los cuatro y doce meses de edad. La geometría del dispositivo se obtuvo a partir de las medidas estadísticas estándar de cráneo para infantes de 6 meses de edad de acuerdo con La Academia Americana de Pediatría y por medio del software GID 8. Los esfuerzos y las deformaciones sufridas por el dispositivo durante su aplicación fueron simuladas por medio de elementos finitos usando el software ANSYS® 10.0. Para estandarizar el tratamiento y conocer la presión aplicada por el dispositivo ortésico en el cráneo del paciente, se elaboró un sensor de presión de aire que trabaja en un intervalo de 0 mm Hg a 55 mm Hg. Los resultados muestran que el dispositivo cumple las especificaciones tanto desde el punto de vista de una validación matemática, como desde las especificaciones del diseño en cuanto a la resolución mínima para las medidas de presión sensadas, confort y resistencia...

This paper presents the development of a prototype orthesis device for the cranium of patientswith positional occipital plagiocephaly. This device will allow the rehabilitation of infants between four months and twelve months old. The device geometry was obtained from statistical cranium measurements evaluated in children of 6 months old by the American Academy of Pediatrics as well through software called GID 8. The stress and strain results were taken from the device during activity, or while the equipment applied some forces on the head; simulations were made by the software of finite element called ANSYS® 10.0. An implementation of air sensor to the device made it possible to know the levels of pressure in a range of 0mm Hg a 55mm Hg. This implementation was done in order to get the standardization of the treatment. The mathematic results as well as the design specifications (minimum resolution of the pressure measurements, comfort and resistance) showed that the device maybe used in rehabilitation.

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