RESUMEN
Cryptorchidism and proximal hypospadia in a newborn are highly suspicious for an intersex disorder, and proper investigations should be planned immediately after birth. In some hypospadic patients, the presence of a palpable gonad in the scrotum may induce to assign the male sex, whereas the anatomy of internal and external genitalia could be extremely complex, requiring an accurate evaluation before any definitive attribution of gender. The authors present a case of an infant, referred to the hospital for surgical treatment of a proximal hypospadia, who showed ambiguous external genitalia, absence of the right gonad, a partially dysgenetic left testis, and presence of both müllerian and wolffian structures. Cytogenetic analysis detected a mosaicism with a cell line showing an isodicentric Yp chromosome and a second one, a 45, X chromosomal complement. Because the baby had been assigned previously to male gender, he underwent a staged masculinizing correction of the genital anomalies. The authors discuss the necessity of a careful evaluation of these patients at birth by a multispecialistic team, for appropriate sex assignment and for the assessment of the risk of neoplastic degeneration.
Asunto(s)
Trastornos del Desarrollo Sexual/diagnóstico , Disgenesia Gonadal Mixta/diagnóstico , Hipospadias/genética , Aberraciones Cromosómicas Sexuales , Cromosomas Humanos Y , Análisis Citogenético , Trastornos del Desarrollo Sexual/genética , Disgenesia Gonadal Mixta/genética , Humanos , Lactante , Masculino , Mosaicismo , Testículo/anatomía & histologíaRESUMEN
To contribute to a better understanding of the role of chromosomal rearrangements in the tumorigenesis of uveal melanoma, we present a case in which a structural aberration of chromosome 3 could indicate the specific region in which an uveal melanoma tumor suppressor gene could be located. We obtained a primary cell culture, characterized by cytogenetic study, through GTG- and CBG-banding techniques by using a mechanical dissection of a tumor sample obtained from an uveal melanoma. Cytogenetic analysis performed in the primary cell culture highlighted the presence of a structural rearrangement involving chromosomes 3 and 22. A t(3;22)(p13;p11) was observed as the only present clonal aberration. The 3p13 breakpoint involved in the aberration observed in our case could be essential in restricting the candidate region for the locus of an uveal melanoma tumor suppressor gene located on chromosome 3.
Asunto(s)
Neoplasias de la Coroides/genética , Aberraciones Cromosómicas , Deleción Cromosómica , Cromosomas Humanos Par 3 , Genes Supresores de Tumor , Melanoma/genética , Neoplasias de la Coroides/patología , Neoplasias de la Coroides/cirugía , Mapeo Cromosómico , Cromosomas Humanos Par 22 , Femenino , Humanos , Cariotipificación , Melanoma/patología , Melanoma/cirugía , Persona de Mediana Edad , Translocación GenéticaRESUMEN
We describe a female child with complex cytogenetic anomalies consisting in partial trisomy of the short arm of chromosome 10, terminal deletion of the long arm of chromosome 2 and--at the same time--a mosaicism for X monosomy. To our knowledge, this is the first case reported in which 10p trisomy is associated to a 2qter deletion. Due to the scarcity of cases reported with pure trisomy, it has not been possible to define the 10p+ syndrome precisely yet. Comparison of our proband's phenotype to both the 2q37 deletion and 10p trisomy showed more features described in 2q37- subjects than in 10p+ ones. We also discuss the difficulties of genetic counseling in children with complex aberrations.
Asunto(s)
Anomalías Múltiples/genética , Aberraciones Cromosómicas/genética , Cromosomas Humanos Par 10 , Cromosomas Humanos Par 2 , Cromosoma X , Deleción Cromosómica , Femenino , Asesoramiento Genético , Humanos , Lactante , Cariotipificación , Monosomía , Fenotipo , TrisomíaRESUMEN
Cytogenetic analyses conducted on several cases of melanoma have contributed to the identification of the chromosomal regions where the sequences responsible for malignant transformation and the evolution of this tumor are probably located. With regard to these problems, it is very important to have the possibility to analyze, through the use of cytogenetics, both the primary melanoma and the metastatic lesions from the same patient. We present a case in which the primary melanoma and five different metastases were studied by using cytogenetics. The primary tumor showed an inversion of chromosome 1 where the p36 region, often proposed in literature as the location of a melanoma susceptibility gene, was involved. Three cutaneous and one lymphonodal metastases presented the same nine clonal chromosomal aberrations. In particular, one is a further rearrangement of the marker present in the primary tumor; another is a deletion of the 9p21pter region in which the p16 gene is located. Our results can provide a contribution to the hypothesis of the location of a candidate gene for melanoma in the 1p36 region and can also underscore the role of the 9p21 region in the progression of melanoma.
Asunto(s)
Aberraciones Cromosómicas , Cromosomas Humanos Par 1 , Melanoma/genética , Neoplasias Cutáneas/genética , Cromosomas Humanos Par 9 , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Masculino , Persona de Mediana Edad , Metástasis de la NeoplasiaRESUMEN
We performed chromosome microdissection in order to define the "de novo" rearrangement observed in a female patient affected by: frontal microgyria, mild psychomotor retardation, thoracic scoliosis, XIIth rib asymmetry and facial dysmorphisms. Through the use of the micro-FISH we evidenced a deletion of the 3p25pter region and a 4p16.1 duplication. We performed a karyotype-phenotype correlation in our patient and in the ones previously reported in literature which had a 3p25pter deletion or the 4p16 duplication.
Asunto(s)
Deleción Cromosómica , Cromosomas Humanos Par 3 , Anomalías Craneofaciales/genética , Reordenamiento Génico/genética , Discapacidad Intelectual/genética , Mapeo Físico de Cromosoma , Adolescente , Bandeo Cromosómico , Femenino , Humanos , Hibridación Fluorescente in Situ , Fenotipo , SíndromeRESUMEN
Recently a new gene called RPGR (retinitis pigmentosa GTPase regulator) was isolated in Xp21.1 and found to be mutated in patients with RP3 type X-linked retinitis pigmentosa. Two new mutations, the first a single base pair deletion and the other a two base pairs deletion, have been found in one Spanish and one Italian family.
Asunto(s)
Proteínas Portadoras/genética , Mutación/genética , Proteínas/genética , Retinitis Pigmentosa/genética , Cromosoma X/genética , Dineínas/genética , Ligamiento Genético , Humanos , Eliminación de SecuenciaRESUMEN
To examine the sensitivity of vitiligo melanocytes to external oxidative stress, we studied enzymatic and non-enzymatic anti-oxidants in cultured melanocytes of normal subjects (n = 20) and melanocytes from apparently normal skin of vitiligo patients (n = 10). The activity of superoxide dismutase and catalase and the intracellular concentrations of vitamin E and ubiquinone were evaluated in cultures at the fourth or fifth passage. In addition, cells were exposed to various concentrations of a peroxidizing agent, cumene hydroperoxide (CUH, 0.66-20 microM), for 1 and 24 h. Compared to normal melanocytes, vitiligo melanocytes showed normal superoxide dismutase and significantly lower catalase activities and higher vitamin E and lower ubiquinone levels. At the concentration used, CUH did not significantly affect cell number or viability of melanocytes after either period of culture. On the contrary, vitiligo melanocytes were susceptible to the toxic effect of CUH after 24 h of continuous treatment at concentrations greater than 6.6 microM. The degree of CUH toxicity correlated strictly with the anti-oxidant pattern, defined as the ratio between vitamin E concentration and catalase activity, suggesting that the alteration in the antioxidants was the basis for sensitivity to the external oxidative stress. Our results demonstrate the presence of an imbalance in the anti-oxidant system in vitiligo melanocytes and provide further support for a free radical-mediated damage as an initial pathogenic event in melanocyte degeneration in vitiligo.
Asunto(s)
Melanocitos/patología , Oxidantes/farmacología , Vitíligo/patología , Adulto , Antioxidantes/farmacología , Derivados del Benceno/farmacología , División Celular/efectos de los fármacos , Células Cultivadas , Femenino , Humanos , Masculino , Melanocitos/efectos de los fármacos , Melanocitos/metabolismo , Persona de Mediana Edad , Estrés Oxidativo , Sensibilidad y Especificidad , Ubiquinona/farmacología , Vitamina E/farmacología , Vitíligo/inducido químicamenteRESUMEN
PURPOSE: To investigate 20 patients affected with Bardet-Biedl (BB) syndrome and compare them to an age-matched group of 70 non-syndromic patients with retinitis pigmentosa (RP) to identify hallmarks peculiar to the BB phenotype. METHODS: Patients were examined clinically and with functional tests (color vision, kinetic perimetry, electroretinography, ocular motility tests). Fundus findings were numerically graded for statistical purposes. RESULTS: Recurrent ocular features in BB patients were early and severe reduction of visual acuity, constantly altered color vision, high incidence of strabismus and nystagmus, mild-to-severe atrophic changes of the optic disc, and frequently absent or minimal pigmentary retinal changes. Visual acuity was more closely correlated to optic disc than to macular conditions. These findings were remarkably different from non-syndromic RP. CONCLUSIONS: This investigation further suggests that retinopathy in BB syndrome has features distinctive from those in non-syndromic RP. The early occurrence of optic disc atrophy in the BB syndrome, even in those patients with healthy maculas, suggests that optic atrophy could often be primary in nature and might play a major role in decreasing central vision in BB patients. Variability of some findings is in line with the documented heterogeneity of the BB syndrome.
Asunto(s)
Anomalías Múltiples/genética , Hipogonadismo/genética , Discapacidad Intelectual/genética , Trastornos de la Motilidad Ocular/genética , Atrofia Óptica/genética , Polidactilia/genética , Retinitis Pigmentosa/genética , Anomalías Múltiples/diagnóstico , Anomalías Múltiples/fisiopatología , Adolescente , Adulto , Niño , Diagnóstico Diferencial , Electrorretinografía , Femenino , Fondo de Ojo , Humanos , Hipogonadismo/diagnóstico , Discapacidad Intelectual/diagnóstico , Masculino , Trastornos de la Motilidad Ocular/diagnóstico , Trastornos de la Motilidad Ocular/fisiopatología , Atrofia Óptica/diagnóstico , Atrofia Óptica/fisiopatología , Fenotipo , Retinitis Pigmentosa/diagnóstico , Retinitis Pigmentosa/fisiopatología , Síndrome , Agudeza Visual , Campos VisualesRESUMEN
We report a case on a female newborn child with a deletion of the 4q33qter region. The patient showed facial dysmorphisms, cleft palate and congenital cardiac defect. In order to contribute to a better definition of the 4q33qter deletion syndrome we have compared the clinical findings of our patient with those in nine reported cases. The characteristic symptoms of these patients seem to be: mental retardation, upper slanting of the palpebral fissures, depressed nasal bridge, low set/dysplastic ears, cleft palate, micrognathia, dysmorphic hands and feet.
Asunto(s)
Deleción Cromosómica , Cromosomas Humanos Par 4 , Discapacidad Intelectual/genética , Femenino , Humanos , CariotipificaciónRESUMEN
Two sibs with multiple congenital anomalies and severe mental retardation were found to have a 2q35qter duplication as a result of a balanced maternal translocation. The clinical features of our two cases are compared with those reported in literature as having either a 2q35qter duplication or a wider duplicated segment without the involvement of any other chromosome deletion or duplication. The typical phenotype is described considering the characteristic clinical features as: hypotonia, hypertelorism, short and beaked nose, flat nasal bridge, thin upper lip, micrognathia, low set and dysmorphic ears, clinodactyly finger V and cryptorchidism.
Asunto(s)
Anomalías Múltiples/genética , Cromosomas Humanos Par 2/genética , Discapacidad Intelectual/genética , Trisomía , Niño , Preescolar , Femenino , Humanos , Masculino , Linaje , FenotipoRESUMEN
In order to evaluate the free radical defense systems of melanocytes and their possible correlation with melanoma, we have studied in cultured normal human melanocytes (20), normal melanocytes from melanoma patients (15), and melanoma cells (40) the fatty acid pattern of membrane phospholipids as a target of peroxidative damage and the superoxide dismutase and catalase activities, vitamin E, and ubiquinone levels as intracellular antioxidants. Cells were cultured in the same medium and analyzed at III or IV passage. Compared to the values obtained in normal human melanocytes, melanoma cells showed on average: a) higher levels of polyunsaturated fatty acids, b) increased superoxide dismutase and decreased catalase activities, higher vitamin E, and lower ubiquinone levels. Among the normal melanocytes from melanoma patients studied, two groups were differentiated: a) cultures (7) with enzymatic and non-enzymatic antioxidants level similar to those of normal human melanocytes; b) cultures (8) with antioxidant patterns similar to those observed in melanoma cells. Polyunsaturated fatty acids were also increased in the latter group. The results indicate that in melanoma cells and in a percentage of normal melanocytes from melanoma patients, an imbalance in the antioxidant system can be detected that can lead to endogenous generation of reactive oxygen species and to cellular incapability of coping with exogenous peroxidative attacks. These alterations could be correlated with the malignant transformation of cells and with the progression of the disease.
Asunto(s)
Antioxidantes/metabolismo , Melanocitos/enzimología , Melanoma/metabolismo , Neoplasias Cutáneas/metabolismo , Adulto , Catalasa/metabolismo , Ácidos Grasos Insaturados/metabolismo , Humanos , Melanoma/patología , Persona de Mediana Edad , Valores de Referencia , Neoplasias Cutáneas/patología , Superóxido Dismutasa/metabolismo , Ubiquinona/metabolismo , Vitamina E/metabolismoRESUMEN
To contribute to the knowledge on tumorigenesis and the evolution of urothelial carcinoma of the ureter, we analyzed the clinical, histological, and cytogenetic aspects of a case. Primary cell cultures obtained from tumor specimens showed a trisomy of chromosome 20 where the c-src proto-oncogene, already described in literature as having an important role in the etiology and progression of some tumors, is located. In our case trisomy 20 is the only present marker and for this reason we think that it could play a role in the tumorigenesis of the urothelial carcinoma of the ureter.
Asunto(s)
Carcinoma Papilar/genética , Cromosomas Humanos Par 20 , Trisomía , Neoplasias Ureterales/genética , Carcinoma Papilar/patología , Carcinoma Papilar/cirugía , Bandeo Cromosómico , Genes src , Humanos , Cariotipificación , Masculino , Persona de Mediana Edad , Invasividad Neoplásica , Proto-Oncogenes Mas , Células Tumorales Cultivadas , Neoplasias Ureterales/patología , Neoplasias Ureterales/cirugía , UrotelioRESUMEN
PURPOSE: To report the clinical and functional characteristics of patients affected with autosomal-dominant transmitted retinitis pigmentosa (adRP) from a large Italian pedigree in which a point mutation predicting the Arg-135-Trp change of rhodopsin was identified by polymerase chain reaction-single-strand conformation polymorphism analysis. METHODS: Seven patients, ranging in age from 6 to 41 years, underwent a full clinical ophthalmologic evaluation, kinetic visual field testing, and electroretinographic testing. RESULTS: In agreement with previous reports, this rhodopsin mutation yielded a particularly severe phenotype, both clinically and functionally. The evaluation of patients from this pedigree in the first and second decade of life demonstrated that retinal function is still electroretinographically measurable at least until 18 years of age, although reduced to 2% to 4% of normal. Longitudinal measures showed that the rate of progression of the disease was unusually high, with an average 50% loss per year of electroretinographic amplitude and visual field area with respect to baseline. Later in the course of the disease, macular function is also severely compromised, leaving only residual central vision by the fourth decade of life. CONCLUSIONS: The phenotype associated with mutations in codon 135 of the rhodopsin molecule appears to have an unusually high progression rate and yields an extremely poor prognosis. These distinctive features make the Arg-135-Trp phenotype substantially different from the general RP population, and also from many of the other adRP pedigrees with known rhodopsin mutations reported to date.
Asunto(s)
Mutación Puntual , Retinitis Pigmentosa/genética , Retinitis Pigmentosa/patología , Rodopsina/genética , Adolescente , Adulto , Arginina/genética , Niño , ADN/análisis , Electrorretinografía , Femenino , Humanos , Estudios Longitudinales , Masculino , Linaje , Fenotipo , Reacción en Cadena de la Polimerasa , Polimorfismo Conformacional Retorcido-Simple , Retina/fisiopatología , Retinitis Pigmentosa/fisiopatología , Triptófano/genética , Campos VisualesRESUMEN
Norrie-Warburg syndrome (NWS) is a rare X-linked disorder characterized by blindness, which is invariable, deafness and mental disturbances, which are present occasionally. We describe here two novel mutations, a missense mutation (C126S) and a 1-base pair insertion (insT466/T467), together with a recurrent mutation (M1V), found in patients presenting with the classical clinical phenotype of NWS. All three mutations are likely to result in prominent structural changes of the norrin protein.
Asunto(s)
Ceguera/genética , Sordera/genética , Trastornos Mentales/genética , Mutación Puntual , Ceguera/congénito , Preescolar , ADN/análisis , Análisis Mutacional de ADN , Ligamiento Genético/genética , Humanos , Masculino , Linaje , Fenotipo , Mutación Puntual/genética , Reacción en Cadena de la Polimerasa , Síndrome , Cromosoma X/genéticaRESUMEN
The authors on the base of two cases of Gardner's syndrome recently observed, proceed to a wide review of literature on this subject so as to stress the peculiar aspects of this syndrome, so complex and uncommon. The greatest emphasis is given to the role of genetics as regarding to diagnosis and screening programs, as well as to the more recent acquisitions about diagnosis, therapy and follow up of risk lesions, such as colorectal and duodenal adenomas, as well as of intrabdominal desmoid tumours, which, although not histologically malignant, may often influence prognosis negatively, because of their remarkable local invasiveness and tendency to recurrence.
Asunto(s)
Síndrome de Gardner , Adulto , Femenino , Síndrome de Gardner/diagnóstico , Síndrome de Gardner/genética , Genotipo , Humanos , Masculino , Linaje , Fenotipo , Tomografía Computarizada por Rayos XRESUMEN
The GRO1 oncogene (melanoma growth-stimulating activity alpha) has been localized in region 4q21. The involvement of this chromosomal region in clonal aberrations found in primary melanoma cell cultures could have an important role in the etiology and pathogenesis of this tumor. We characterized three primary cell cultures obtained from different patients, each of which showed clonal chromosomal aberrations involving the 4q21 region.
Asunto(s)
Quimiocinas CXC , Aberraciones Cromosómicas , Cromosomas Humanos Par 4 , Péptidos y Proteínas de Señalización Intercelular , Melanoma/genética , Neoplasias Cutáneas/genética , Quimiocina CXCL1 , Factores Quimiotácticos/genética , Citogenética , Sustancias de Crecimiento/genética , Humanos , Técnicas para Inmunoenzimas , Melanoma/química , Proteínas de Neoplasias/genética , Neoplasias Cutáneas/química , Células Tumorales CultivadasRESUMEN
BACKGROUND: The variability of the visual function impairment in dominant optic atrophy (DOA) makes it difficult to diagnose the disease within genealogies. Physiologic investigations were conducted on a family with DOA to evaluate methods of detecting clinical and subclinical signs in obligate heterozygotes, in order to identify affected subjects within the genealogy and to formulate the individual and reproductive risks. METHODS: Investigations included tests for color vision, contrast sensitivity function (CSF), kinetic and static computerized perimetry, transient pattern reversal visual evoked potentials (VEPs) and steady-state flash VEPs. RESULTS: Eight subjects from the pedigree were diagnosed as having DOA. Two of them were unaware of their affection, and six showed wide clinical variability. CSF paralleled the central visual impairment, but was also slightly impaired in the two unaware subjects. Static computerized perimetry disclosed mild sensitivity defects in the central visual fields in these two patients. VEPs showed heterogeneous results as well, ranging from normal findings to severely altered tracings. CONCLUSIONS: This investigation suggests that combined clinical and functional evaluation is necessary to diagnose DOA. Particularly, the combined use of computerized perimetry, CSF, and VEPs allowed the identification of cases at a subclinical stage.
Asunto(s)
Percepción de Color/fisiología , Sensibilidad de Contraste/fisiología , Potenciales Evocados Visuales/fisiología , Atrofias Ópticas Hereditarias/diagnóstico , Atrofias Ópticas Hereditarias/fisiopatología , Campos Visuales/fisiología , Adolescente , Adulto , Femenino , Genes Dominantes , Humanos , Masculino , Persona de Mediana Edad , Linaje , Estimulación Luminosa , Pruebas del Campo VisualRESUMEN
One of the primary goals in medical genetics is a precise clinical definition of chromosomal diseases. This is now possible because of the increased number of case reports and new techniques. A male patient, without a clear-cut syndrome, was cytogenetically investigated. Chromosomal analysis showed a small unidentified bisatellited supernumerary marker. In situ hybridization with a biotin-labeled DNA probe for the chromosome 15 centromere (D15Z1) demonstrated that the marker was derived from chromosome 15. Hybridization with the Prader-Willi Syndrome Cosmid biotinylated probe (localized to band 15q11-q13) showed a signal on both ends suggesting a marker with a symmetrical inv dup(15) and a breakpoint localized in q13. It was then possible to define the karyotype as: 47,XY,+ inv dup(15) (pter-q13::q13-pter). All cases of inv dup(15) reported in the literature were reviewed, paying particular attention to the different breakpoints involved, in order to provide a better clinical definition of this syndrome.
Asunto(s)
Inversión Cromosómica , Cromosomas Humanos Par 15 , Familia de Multigenes/genética , Adolescente , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Masculino , FenotipoRESUMEN
Congenital bilateral microphthalmos is a rare malformation of the eye, which ranges from extreme to mild reduction of total axial length. Microphthalmos may occur as an isolated ocular abnormality or as part of a systemic disorder, and different classifications of the condition have been attempted. We describe a large pedigree with 14 persons in four generations affected with bilateral microphthalmos without other ocular or systemic signs. An autosomal dominant trait with complete penetrance is proposed. Five subjects underwent a complete ophthalmological evaluation. The total axial length was measured by A scan ultrasonography in all persons. Ultrasonography showed a reduction of the total axial length (range 18.4-19.7 mm) and a reduced vitreous cavity length (range 11.4-13.5 mm) in all investigated patients. All the patients had microcornea (range 8-9.7 mm). No other ocular anomalies or associated systemic malformations were found. A review of published reports also suggests that simple, partial, posterior, pure microphthalmos and nanophthalmos are similar clinical entities sharing total axial length and vitreous cavity length reduction. Therefore, the term simple microphthalmos is proposed to identify these clinical conditions.
Asunto(s)
Microftalmía/genética , Adulto , Anciano , Niño , Femenino , Genes Dominantes , Humanos , Masculino , Persona de Mediana Edad , LinajeRESUMEN
The NM23 gene has been proposed as a metastasis-suppressor gene, and its use has been suggested as prognostic factor. NM23 was identified in a system of murine melanoma cell lines, in which an inverse relationship was found between NM23 expression and metastatic ability. In a human malignant melanoma study NM23 expression was found to be significantly lower in metastases that developed less than 24 months after diagnosis of the primary tumours. The present paper studies the expression of the NM23.H1 gene in cell lines which derive from primary or metastatic human malignant melanomas in relation to staging, infiltration degree, lymphocytic infiltration, cell morphology, cell pigmentation, karyotype, and disease-free survival. The level of mRNA expression of the NM23 gene is significantly lower in cell lines that derive from more infiltrating primary melanomas than in cell lines obtained from less infiltrating tumours. Moreover, cell lines derived from tumours of patients with a disease-free survival of more than 24 months (24-58 months) express the NM23 gene at higher levels than cell lines obtained from melanomas of patients with a disease-free survival of less than 24 months (6-15 months).