RESUMEN

OBJECTIVE: To evaluate the postoperative sensitivity (POS), as well as the clinical performance of posterior restorations using a new chemically-cured bulk-fill composite (Stela Automix and Stela Capsule, SDI) comparing with a light-cured bulk-fill composite after 6 months. METHODS: Fifty-five participants with at least three posterior teeth needing restoration were recruited. A total of 165 restorations were performed on Class I or Class II cavities. After the application of Stela primer, the chemically-cured composite (Stela Automix or Stela Capsule) was inserted. For the light-cured composite group, a universal adhesive (Scotchbond Universal) was applied with a bulk-fill composite (Filtek One). Participants were evaluated for spontaneous and stimulated POS in the baseline, after 48 h, 7 days, and 6 months. Additionally, each restoration was assessed using the updated version of FDI criteria after 6 months. The differences in the proportions of the groups were compared by Cochran test statistics (α = 0.05). RESULTS: Both chemically-cured composites showed a lower risk of POS compared to the light-cured composite at baseline and up to 48 h (p < 0.04). A significantly lower surface luster and texture was observed for the Stela Capsule composite compared to the light-cured bulk-fill composite (baseline and 6 months; p = 0.03). A significant color mismatch was observed for the light-cured bulk-fill composite compared to the chemically-cured composites (baseline and 6 months; p = 0.03). No significant differences were observed in any other item evaluations (p > 0.05). CONCLUSION: Chemically-cured composites exhibit lower postoperative sensitivity and less color mismatch compared to a light-cured bulk-fill composite after 6 months of clinical service. CLINICAL SIGNIFICANCE: The chemically-cured composites appear to be an appealing option for restoring posterior teeth, as they exhibit lower postoperative sensitivity compared to a light-cured bulk-fill composite, both at baseline and up to 48 h, and less color mismatch.

Asunto(s)

RESUMEN

Benign acute childhood myositis (BACM) is a rare clinical condition that mainly affects pre-school and school age-children. It is usually preceded by a viral illness, particularly influenza virus infection. OBJECTIVE: To describe a cluster of BACM cases that were seen in a paediatric unit. PATIENTS AND METHODS: A retrospective series of cases that presented with a clinical picture suggestive of BACM between August and November 2012 in the paediatric emergency department of a private clinic. RESULTS: Nine children, between 4 and 12 years, presented with a history of a recent febrile upper viral respiratory infection, followed by intense calf pain and claudication. They all recovered without complications. Laboratory results showed a marked increase in CK, with a mean of 4,066 IU/l. Three of the cases had influenza B infection and one Mycoplasma pneumonia infection. They were managed conservatively with hydration and non-steroidal anti-inflammatory drugs. CONCLUSIONS: BACM is a benign entity with a characteristic clinical presentation that can be managed most of the time in the ambulatory setting, avoiding invasive studies and unnecessary hospital admission.

Asunto(s)

RESUMEN

La miositis aguda benigna de la infancia (MABI) es una entidad clínica autolimitada, infrecuente, que afecta a niños en edad preescolar y escolar. Dada su asociación a cuadros virales, se sugiere una relación con este tipo de agentes, entre los que predomina el virus influenza. OBJETIVO: Describir un brote de casos de MABI presentados en un servicio pediátrico. PACIENTES Y MÉTODO: Serie clínica retrospectiva de pacientes que consultaron por un cuadro clínico compatible con MABI en el período agosto-noviembre de 2012, en el Servicio de Urgencia pediátrico de un centro asistencial. RESULTADOS: Se presentan una serie de 9 niños, edades entre 4 y 12 años, con un pródromo de fiebre asociado a síntomas respiratorios, seguido de dolor agudo intenso de ambas pantorrillas y claudicación. En los exámenes de laboratorio destacaba un alza de creatincinasa, con un valor promedio de 4.066 UI/L. El estudio etiológico evidenció influenza B en 3 pacientes y Mycoplasma pneumoniae en uno. El manejo consistió en hidratación y antiinflamatorios no esteroidales, con favorable evolución clínica y de laboratorio. CONCLUSIONES: La MABI es una entidad benigna, autolimitada, de excelente pronóstico, con una presentación clínica que en la mayoría de los casos requiere manejo ambulatorio. Deben evitarse estudios invasivos y hospitalizaciones innecesarias.

Benign acute childhood myositis (BACM) is a rare clinical condition that mainly affects pre-school and school age-children. It is usually preceded by a viral illness, particularly influenza virus infection. OBJECTIVE: To describe a cluster of BACM cases that were seen in a paediatric unit. PATIENTS AND METHODS: A retrospective series of cases that presented with a clinical picture suggestive of BACM between August and November 2012 in the paediatric emergency department of a private clinic. RESULTS: Nine children, between 4 and 12 years, presented with a history of a recent febrile upper viral respiratory infection, followed by intense calf pain and claudication. They all recovered without complications. Laboratory results showed a marked increase in CK, with a mean of 4,066 IU/l. Three of the cases had influenza B infection and one Mycoplasma pneumonia infection. They were managed conservatively with hydration and non-steroidal anti-inflammatory drugs. CONCLUSIONS: BACM is a benign entity with a characteristic clinical presentation that can be managed most of the time in the ambulatory setting, avoiding invasive studies and unnecessary hospital admission.

Asunto(s)

RESUMEN

INTRODUCTION: Congenital syphilis (CS) is a multisystemic infection of the newborn (NB) which can produce severe symptoms, and in some cases, even be fatal. In recent years, the incidence of syphilis has increased worldwide and similarly, the cases of CS in neonates have increased. OBJECTIVE: To report two cases of early and severe presentation of CS, focusing on the importance of prevention of vertical transmission and monitoring of treated mothers. The diagnostic difficulties are discussed. CLINICAL CASES: Two premature newborns that were diagnosed with probable CS present in the newborn period are presented. In the first case, due to a high index of suspicion, but without confirmatory testing, treatment was started with good clinical response. In the second case, CS was confirmed through positive serology and the specific treatment was given. CONCLUSION: CS has significant diagnostic challenges as there is no test for early confirmation, therefore, a high index of suspicion might be key in the treatment and consequent prognosis. Due to the current epidemiology of the condition, it is also important to focus on preventive measures.

Asunto(s)

RESUMEN

Introduction: Congenital syphilis (CS) is a multisystemic infection of the newborn (NB) which can produce severe symptoms, and in some cases, even be fatal. In recent years, the incidence of syphilis has increased worldwide and similarly, the cases of CS in neonates have increased. Objective: To report two cases of early and severe presentation of CS, focusing on the importance of prevention of vertical transmission and monitoring of treated mothers. The diagnostic difficulties are discussed. Clinical cases: Two premature newborns that were diagnosed with probable CS present in the newborn period are presented. In the first case, due to a high index of suspicion, but without confirmatory testing, treatment was started with good clinical response. In the second case, CS was confirmed through positive serology and the specific treatment was given. Conclusion: CS has significant diagnostic challenges as there is no test for early confirmation, therefore, a high index of suspicion might be key in the treatment and consequent prognosis. Due to the current epidemiology of the condition, it is also important to focus on preventive measures.

Introducción: La sífilis congénita (SC) es una infección multisistémica que afecta al recién nacido (RN) y que puede producir manifestaciones clínicas de variada gravedad, e incluso ser fatal. Durante los últimos años, la incidencia de la sífilis ha aumentado a nivel mundial y, de igual forma, la SC en neonatos. Objetivo: Reportar 2 casos de presentación precoz y grave de SC, recalcando la importancia de la prevención de la trasmisión vertical y el seguimiento de las madres tratadas. Se discuten las dificultades diagnósticas. Casos clínicos: Se presentan dos RN prematuros, a quienes se les diagnosticó una probable SC durante su período neonatal inmediato. En el primer caso, debido a un alto índice de sospecha, aunque sin exámenes confirmatorios, se inició tratamiento, con buena respuesta clínica. En el segundo caso se confirmó diagnóstico de SC con serología, permitiendo el tratamiento específico. Conclusiones: La SC presenta un desafío diagnóstico importante dado que no existe un examen que permita su confirmación precoz, por lo que un alto índice de sospecha puede ser determinante en la oportunidad de tratamiento y consecuente pronóstico. Considerando la epidemiología actual, parece importante, además, reforzar las medidas de prevención a nivel pre concepcional.

Asunto(s)

RESUMEN

Objective: This study evaluates the diagnostic value of Renal Doppler Ultrasound (RDU) in the diagnosis of acute renal involvement among children admitted for a first febrile urinary tract infection (UTI), compared to a Renal Scintigraphy (RS). Methodology: All children admitted during 2009 for a first febrile UTI and positive urinary culture were prospectively studied. All received a RDU and RS with Tc99di-mercaptosuccinic acid during the first 72 hours of hospitalization. Image evaluation was performed blindly. RS was considered to be the gold standard to identify renal involvement. Results: The protocol was completed in 54 children (90 percent). RDU was altered in 36 (66 percent), and RS in 42 (78 percent) of children. Both exams coincided in 78 percent of the children, and in 81 percent of the kidneys. Sensitivity and specificity of RDU for these patients was 78,6 percent and 75 percent (72 percent and 89,6 percent per kidney), respectively. Negative predictive value was 50 percent. RDU detected significantly fewer defects in the left kidney, (p = 0,0026), especially if the defect was localized in the upper pole, and in absence of other associated scintigraphic abnormalities (p = 0,0001). Children with scintigraphic renal involvement showed significant more alterations during the acute phase. Conclusions: RDU is sensitive and specific to detect renal involvement in a child admitted for a febrile UTI, but has a low negative predictive value. Therefore, a negative ultrasound in a patient with inflammatory signs should be confirmed through a scintigraphy, since there are certain sites that are difficult to localize in a sonogram, such as the left superior pole.

Introducción: El objetivo del presente estudio fue evaluar las propiedades diagnósticas de la ecografía renal con Doppler (ERD) en la identificación del compromiso renal agudo, en una cohorte de niños hospitalizados con primera infección urinaria (ITU) febril y compararlas con el cintigrama renal estático (CR). Metodología: Durante el año 2009, en forma prospectiva, se estudiaron todos los niños hospitalizados con primera ITU febril y con urocultivo positivo. En todos ellos se realizó una ERD y un CR con ácido dimercapto succínico marcado con tecnecio 99, dentro de las primeras 72 horas de hospitalización. Los estudios de imágenes fueron realizados en forma ciega, por operadores independientes. El CR se consideró como gold standard para la identificación de compromiso renal. Resultados: En 54 niños (90 por ciento de los elegibles) hospitalizados por ITU febril se cumplió el protocolo de estudio imageneológico. La ERD estuvo alterada en 36 (66 por ciento) y el CR en 42 (78 por ciento) de los niños. Ambos exámenes fueron coincidentes en 78 por ciento de los niños y en 81 por ciento de los riñones estudiados. La sensibilidad y especificidad del la ERD para estos pacientes fueron de 78,6 por ciento y 75 por ciento (72 por ciento y 89,6 por ciento al analizarlo por unida renal), respectivamente, y el valor predictivo negativo de 50 por ciento. La ERD pesquisó significativamente menos defectos cuando éstos eran exclusivos del riñón izquierdo (p = 0,0026), especialmente si el defecto se localizó en el polo superior y en ausencia de otras alteraciones cintigráficas asociadas (p = 0,0001). Los niños con compromiso renal cintigráfico tenían significativamente más alterados los reactantes de fase aguda. Conclusiones: La ERD en un niño hospitalizado por una ITU febril tiene alta sensibilidad y especificidad para pesquisar el compromiso renal, pero un bajo valor predictivo negativo; por lo tanto, si la ERD es negativa y el paciente presenta parámetros inflamatorios alterados, el compromiso renal debe ser confirmado por un CR, ya que existe evidencia de ciertas localizaciones más difíciles de identificar por la ERD, como aquellas que afectan el polo superior izquierdo.

Asunto(s)

RESUMEN

Tumor lysis syndrome is a metabolic emergency resulting from the rapid and massive destruction of tumor cells, spontaneously or secondary to cytolytic therapy for cancer. This results in a huge imbalance of internal environment by releasing large amounts of intracellular contents into the interstitial and intravascular space, with serious clinical consequences or even death. The pediatric population is especially at risk of tumor lysis syndrome because it has a high rate of fast-growing tumors, such as those of hematologic origin. Proper recognition of the risk factors that can cause this syndrome, as well as specific prevention and treatment has substantially decreased complications and improved survival in these patients.

El síndrome de lisis tumoral es una emergencia metabólica derivada de la rápida y masiva destrucción de células tumorales en forma espontánea o secundaria a terapia citolítica del cáncer. Esta situación produce un enorme desequilibrio del medio interno al liberarse grandes cantidades de contenido intracelular al espacio intersticial e intravascular, con consecuencias clínicas serias e incluso mortales. La población pediátrica está especialmente expuesta a sufrir síndrome de lisis tumoral ya que presenta una tasa elevada de tumores de rápido crecimiento, como son los de orígenes hematológicos. El adecuado reconocimiento de los factores de riesgo que pueden causar este síndrome, así como su prevención y tratamiento específicos han disminuido sustancialmente las complicaciones y mejorado la sobrevida de estos pacientes.

Asunto(s)

RESUMEN

Clinical and epidemiological aspects of shigatoxin producing E. coli (STEC) infections and hemolytic uremic syndrome (HUS) are reviewed. Surveillance results from 14 sentinel centers during 2000-2002 showed a mean incidence rate of 3.4 HUS cases per 100.000 children, with the highest incidence in the 6 to 28 month age group. Disease is endemic with summer peaks. Between 1988 and 2002 we obtained the clinical characteristics of a group of 119 HUS children with the following results: mean age 16 months, bloody diarrhea 57.8 percent, no previous diarrhea 9 percent, 60 percent received antibiotics, 72 percent had oligoanuria, 53 percent required dialysis, 15 percent had seizures and 31 percent had dizziness; mortality was 3 percent. Four foodborne outbreaks have been detected in Santiago, two outbreaks occurred in household settings, one in a Day Care Center and one in a Neonatal Unit. Recommendations for diagnosis, treatment and prevention of STEC infections, including potential vaccines are discussed.

Se revisan y actualizan aspectos clínicos y epidemiológicos de las infecciones por Escherichia coli productora de shigatoxina (STEC), y el síndrome hemolítico urémico (SHU). Se incluyen resultados de una vigilancia de SHU en 14 centros centinelas (2000-2002), que mostró una incidencia promedio de 3,4 casos por 100.000 niños, 78 por ciento) en el grupo de 6 a 48 meses. Esta vigilancia reflejó una situación endémica, con aumento en verano. Se analiza la observación clínica protocolizada de 119 pacientes con SHU hospitalizados en la Región Metropolitana (RM) (1988 y 2002). Edad promedio: 16 meses. El 578 por ciento> tenía diarrea con sangre, 9 por ciento> no tenía diarrea previa, 60 por ciento> recibió antibacterianos, 72 por ciento> presentó oligoanuria y 53 por ciento> necesitó diálisis. El 31 por cientoo tuvo compromiso de conciencia y 15 por cientoo presentó convulsiones. Letalidad 3 por ciento. Se analizan brotes de STEC asociados a alimentos ocurridos en la RM en el hogar (2), un jardín infantil (1) y en un servicio de neonatología (1). Finalmente, se entregar recomendaciones para el manejo clínico y prevención, se revisan los criterios diagnósticos, nuevas estrategias terapéuticas y progresos en el desarrollo de vacunas.

Asunto(s)

RESUMEN

Background: Hemolytic-uremic syndrome (HUS) is characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. Aim: To describe the characteñstics ofpatients with the diagnosis ofHUS in Chile, and to identify the most reliable early predictors oímorbidity and moñality. Material and methods: The clinical records ofpatients with HUS aged less than 15 years, attended between January 1990 and December 2003 in 15 hospitals, were reviewed. Demographic, clinical, biochemical, hematological parameters, morbidity and mortality were analyzed. Results: A cohort of 587 patients aged 2 to 8 years, 48 percent males, was analyzed. Ninety two percent had diarrhea. At the moment of diagnosis, anuria was observed in 39 percent of the patients, hypertension in 45 percent and seizures in 17 percent. Forty two percent required renal replacement therapy (RRT) and perítoneal dialysis was used in the majoríty of cases (78 percent). The most frequently isolated etiological agentwas Escherichia coli. Mortality rate was 2.9 percent in the acute phase of the disease and there was a positive correlation between mortality and anuria, seizures, white blood cell count (WCC) >20.000/mm³ and requirements of renal replacement therapy (p <0.05). Twelve percent of patients evolved to chronic renal failure and the risk factors during the acute phase were the need for renal replacement therapy, anuria, WCC >20.000/mm³, seizures and hypertension. Conclusions: The present study emphasizes important clinical and epidemiological aspeets ofHUSin a Chilean pediatricpopulation.

Asunto(s)

Asunto(s)

Asunto(s)

RESUMEN

Clinical and epidemiological aspects of shigatoxin producing E. coli (STEC) infections and hemolytic uremic syndrome (HUS) are reviewed. Surveillance results from 14 sentinel centers during 2000-2002 showed a mean incidence rate of 3.4 HUS cases per 100,000 children, with the highest incidence in the 6 to 28 month age group. Disease is endemic with summer peaks. Between 1988 and 2002 we obtained the clinical characteristics of a group of 119 HUS children with the following results: mean age 16 months, bloody diarrhea 57.8%, no previous diarrhea 9%, 60% received antibiotics, 72% had oligoanuria, 53% required dialysis, 15% had seizures and 31% had dizziness; mortality was 3%. Four foodborne outbreaks have been detected in Santiago, two outbreaks occurred in household settings, one in a Day Care Center and one in a Neonatal Unit. Recommendations for diagnosis, treatment and prevention of STEC infections, including potential vaccines are discussed.

Asunto(s)

RESUMEN

BACKGROUND: Hemolytic-uremic syndrome (HUS) is characterized by acute renal failure, microangiopathic hemolytic anemia and thrombocytopenia. AIM: To describe the characteristics of patients with the diagnosis of HUS in Chile, and to identify the most reliable early predictors of morbidity and mortality. MATERIAL AND METHODS: The clinical records of patients with HUS aged less than 15 years, attended between January 1990 and December 2003 in 15 hospitals, were reviewed. Demographic, clinical, biochemical, hematological parameters, morbidity and mortality were analyzed. RESULTS: A cohort of 587 patients aged 2 to 8 years, 48% males, was analyzed. Ninety two percent had diarrhea. At the moment of diagnosis, anuria was observed in 39% of the patients, hypertension in 45% and seizures in 17%. Forty two percent required renal replacement therapy (RRT) and peritoneal dialysis was used in the majority of cases (78%). The most frequently isolated etiological agent was Escherichia coli. Mortality rate was 2.9% in the acute phase of the disease and there was a positive correlation between mortality and anuria, seizures, white blood cell count (WCC)>20.000/mm3 and requirements of renal replacement therapy (p<0.05). Twelve percent of patients evolved to chronic renal failure and the risk factors during the acute phase were the need for renal replacement therapy, anuria, WCC>20.000/mm3, seizures and hypertension. CONCLUSIONS: The present study emphasizes important clinical and epidemiological aspects of HUS in a Chilean pediatric population.

Asunto(s)

RESUMEN

El Síndrome de Mala Eliminación (SME) comprende la alteración en la evacuación a nivel intestinal y urinario, en distintos grados y formas de presentación clínica. Diversos estudios muestran el origen de esta patología en una alteración a nivel de la musculatura del piso pelviano. El objetivo de esta revisión es entregarle al pediatra una visión general de este concepto, usa cada vez más utilizado en la literatura internacional, destacando la importancia de la sospecha clínica, diagnóstico y manejo precoz. Los resultados de estudios internacionales avalan la necesidad del tratamiento conjunto de la afección urinaria y gastrointestinal, para lograr mayor porcentaje de mejoría. El enfoque conjunto de la incontinencia y la constipación, más la amplia gama de situaciones clínicas que cada uno de ellos conlleva, es el objetivo que persigue introducir este nuevo síndrome.

Asunto(s)

RESUMEN

Antecedentes: Durante los años 80 y 90 se crearon en Chile diversos programas para reducir la morbimortalidad por insuficiencia renal crónica (IRC) en niños y adolescentes. Objetivo: Describir la evolución de la mortalidad y proporción de muertes por IRC en un período de 20 años. Material y Métodos: Se calculó la tasa de mortalidad y proporción de muertes por IRC para cada año del período 1984–2003 en pacientes menores de 19 años. Se analizó su evolución temporal mediante la comparación del riesgo de fallecer por IRC en los trienios extremos (1984-1986 y 2001-2003); similar metodología se empleó para caracterizar la evolución temporal de la proporción de muertes por IRC. Resultados: El riesgo de fallecer por IRC en el trienio 1984-1986 fue 3,7 veces mayor al riesgo del trienio 2001-2003 (p = 0,01). La comparación de la proporción de muertes por IRC no presentó diferencias entre los trienios extremos (p = 0,68). Conclusión: La tasa de mortalidad por IRC en niños y adolescentes disminuyó entre 1984 y 2003, a diferencia de la proporción de muertes por IRC, la cual permaneció invariable. Este comportamiento estaría explicado tanto por una disminución de la mortalidad por IRC de manera proporcional a la mortalidad por otras causas de mayor incidencia (ej. enfermedades infecciosas) como por un desplazamiento de su ocurrencia a edades mayores.

Asunto(s)

RESUMEN

Los fenómenos tromboembólicos en pacientes con síndrome nefrótico constituyen una de las complicaciones más temidas debido al riesgo vital asociado. Objetivo: Describir los principales mecanismos fisiopatológicos responsables del desarrollo de este tipo de complicación a propósito de cuatro casos clínicos, en tres de los cuales se describen fenómenos tromboembólicos cerebrales y en uno trombosis extensa de extremidad inferior asociado a dificultad respiratoria. Las interacciones entre cuatro condiciones: actividad desbalanceada entre moléculas procoagulantes y anticoagulantes, trombocitosis, hiperagregación plaquetaria e hiperviscosidad sanguínea, promueven un estado de hipercoagulabilidad que conduce al desarrollo de complicaciones tromboembólicas, sin embargo, los mecanismos fisiopatólogicos subyacentes no han sido completamente aclarados. La presencia de otros factores tales como infecciones, complejos inmunes circulantes, hipovolemia, hipertensión, terapia esteroidal, punciones venosas e inmovilización pueden jugar un rol en la trombogénesis asociada al síndrome nefrótico. Conclusión: El síndrome Nefrótico representa una condición de alto riesgo de tromboembólismo, y requiere consideraciones terapéuticas tales como el uso criterioso de diuréticos, prevención de infecciones, mantenimiento de niveles adecuados de albúmina y el uso de fármacos antiplaquetarios y/o anticoagulantes.

Asunto(s)

RESUMEN

La actividad deportiva ha ido ganando adeptos en nuestro país, sin hacer diferencias entre grupos socio-económicos ni por edades. Los beneficios que aporta esta actividad física son ampliamente reconocidos y tienden a mejorar la calidad de vida de quienes la realizan, pero la práctica de estos mismos deportes puede tener efectos adversos, mas allá de las clásicas lesiones ortopédicas y/o traumatológicas. Ya sea por la agresividad del deporte en sí, la demanda física excesiva que requiere, o por condiciones de salud personales, esta actividad puede alterar la función o lesionar otros sistemas u órganos. En este artículo se revisan los efectos adversos que pueden tener algunos deportes o actividad física sobre el riñón -sano y enfermo-, y sobre algunos parámetros de regulación homeostática renal, con especial énfasis en la edad pediátrica.

Asunto(s)

Asunto(s)

Asunto(s)

RESUMEN

Background:Hemolytic uremic syndrome (HUS) is one of the main causes of acute renal failure in the Chilean pediatric population. Aim: To report the features of patients with HUS, admitted to the pediatric ward of a clinical hospital. Material and methods: Retrospective review of medical records of patients admitted with the diagnosis of HUS between 1995 and 2002. Results: During the period, 58 patients were admitted with the diagnosis of HUS but only 43 (age range 1 month to 6 years, 22 females) had complete medical records for review. Ninety five percent presented with prodromic diarrhea, mainly dysenteric. Antibiotics were administered to 70%, in the previous days. Acute renal replacement, mainly peritoneal dialysis, was required in 40%. The clinical signs and laboratory parameters that correlated better with the indication for dialysis were anuria, hypertension, initial and permanently high serum creatinine and blood urea nitrogen. Four patients with blood urea nitrogen over 100 mg/dl but without anuria or hyperkalemia, were treated conservatively, and experienced an uneventful course (permissive azotemia). Hospital stay was almost 3 times greater in dialyzed than in non dialyzed children. No deaths related to HUS were reported in the study period. In an average follow up of 54 months, 11.6% of the patients developed chronic renal failure of diverse magnitude. Conclusions: Despite the fact that our study group behaved clinically similar to published HUS patients in other series, no mortality was observed in a retrospective analysis of patients with this disease.

Asunto(s)