RESUMEN
BACKGROUND: Males have higher weight and length at birth than females. AIM: To verify the influence of the Y chromosome and the action of intrauterine androgens on weight and length at birth of children with Disorders of Sex Development (DSD). SUBJECTS AND METHODS: A cross-sectional and retrospective study. Patients with Turner syndrome (TS), complete (XX and XY), mixed (45,X/46,XY) and partial (XY) gonadal dysgenesis (GD), complete (CAIS) and partial (PAIS) androgen insensitivity syndromes and XX and XY congenital adrenal hyperplasia (CAH) were included. Weight and length at birth were evaluated. RESULTS: Weight and length at birth were lower in TS and mixed GD when compared to XY and XX DSD cases. In turn, patients with increased androgen action (117 cases) had higher weight and length at birth when compared to those with absent (108 cases) and decreased (68 cases) production/action. In birthweight, there was a negative influence of the 45,X/46,XY karyotype and a positive influence of increased androgen and gestational age. In birth length, there was a negative influence of the 45,X and 45,X/46,XY karyotypes and also a positive influence of increased androgen and gestational age. CONCLUSIONS: The sex dimorphism of weight and length at birth could possibly be influenced by intrauterine androgenic action.
Asunto(s)
Síndrome de Resistencia Androgénica , Andrógenos , Masculino , Niño , Recién Nacido , Femenino , Humanos , Estudios Retrospectivos , Caracteres Sexuales , Estudios TransversalesRESUMEN
BACKGROUND: The aim of this study was to investigate the frequency of gonadal tumors among patients with Turner syndrome (TS) carrying Y-derivative sequences in their chromosomal constitution. METHODS: Six out of 260 patients with TS were selected based on mosaicism of the entire Y chromosome; 10 were included because Y-derivative sequences have been detected by PCR with specific oligonucleotides (sex-determining region on the Y, testis specific-protein, Y and DYZ3) and further confirmed by FISH. The 16 patients were subjected to bilateral gonadectomy at ages varying from 8.7 to 18.2 years. Both histopathological investigation with hematoxylin and eosin (H&E) and immunohistochemical analysis with anti-octamer-binding transcription factor 4 (OCT4) antibody were performed. RESULTS: Gonadal neoplasia was not detected in any of the 32 gonads evaluated by H&E; however, four gonads (12%) from three patients (19%) had positive OCT4 staining in 50-80% of nuclei, suggesting the existence of germ cell tumors (gonadoblastoma or in situ carcinoma). CONCLUSIONS: Evaluation of the real risk of development of gonadal tumors in TS patients with Y-derivative sequences in their chromosomal constitution may require a specific histopathological study, such as immunohistochemistry with OCT4.
Asunto(s)
Carcinoma in Situ/genética , Cromosomas Humanos Y/química , Gonadoblastoma/genética , Factor 3 de Transcripción de Unión a Octámeros/metabolismo , Síndrome de Turner/genética , Adolescente , Carcinoma in Situ/complicaciones , Carcinoma in Situ/patología , Niño , Cromosomas Humanos Y/genética , Femenino , Gonadoblastoma/complicaciones , Gonadoblastoma/patología , Humanos , Inmunohistoquímica , Medición de Riesgo , Síndrome de Turner/complicaciones , Síndrome de Turner/patologíaRESUMEN
BACKGROUND: Congenital perineal lipoma is extremely rare and may lead to a misdiagnosis of ambiguous genitalia. CASE REPORTS: We report on two girls referred to our service for ambiguous genitalia. Patient 1 (17 days old) and patient 2 (2 months old) had unremarkable gestational and perinatal histories. Both had normal female external genitalia and a 46,XX karyotype. Patient 1 had a polypoid, protruding 3.0 x 2.0 x 1.5-cm phallic-like mass arising at the inferior border of the left labium majora, and patient 2 had a similar mass of 1.5 x 1.5 x 1.0 cm at the same site and an imperforate anus. In both cases the mass was removed and found to be a lipoma. DISCUSSION: To our knowledge, perineal lipoma has been reported only in eleven girls, nine of them with associated anorectal malformation. Migration and fusion of the labioscrotal folds and formation of the urorectal septum are simultaneous developmental events occurring in the same region, which may explain the association of perineal lipoma and anorectal malformations.
Asunto(s)
Lipoma/congénito , Perineo , Ano Imperforado/epidemiología , Femenino , Genitales Femeninos/embriología , Humanos , Recién Nacido , CariotipificaciónRESUMEN
Male to female sex reversal results from failure of testis development. Mutations in the SRY gene or in other genes involved in the sexual differentiation pathway are considered to cause XY gonadal dysgenesis. The majority of the mutations in the SRY described so far are located within the SRY coding region, mainly in the HMG-box conserved domain. Comparison of 5' flanking SRY gene sequences among different species indicated the presence of several putative conserved consensus sequences for different transcription regulators. In this study, we investigated a 360 bp sequence encompassing the SRY putative core promoter, in 17 patients with variable degrees of 46,XY sex reversal, which have been previously shown not to bear mutations in the SRYcoding region. Sequencing analysis of the SRYpromoter in one patient with complete XY gonadal dysgenesis revealed a three base pair deletion in one of the Sp1 binding sites. The deletion abolished Sp1 binding in vitro. This is the first report on a naturally occurring mutation affecting the Sp1 regulatory element in the SRY promoter region, which is associated with sex reversal. Additionally, upon familial investigation the father, who had 18 genital surgeries due to severe hypospadia without cryptorchidism, was found to bear the same deletion and several relatives were referred to have sexual ambiguity.
Asunto(s)
Trastornos del Desarrollo Sexual , Eliminación de Gen , Genes sry , Regiones Promotoras Genéticas , Factor de Transcripción Sp1/metabolismo , Adolescente , Adulto , Secuencia de Bases , Sitios de Unión , Femenino , Gónadas/anatomía & histología , Gónadas/fisiología , Humanos , Masculino , Datos de Secuencia Molecular , Mutación , Linaje , Unión Proteica , Alineación de SecuenciaRESUMEN
BACKGROUND: EEM syndrome is the rare association of ectodermal dysplasia, ectrodactyly, and macular dystrophy. METHODS: We here demonstrate through molecular analysis that EEM is caused by distinct homozygous CDH3 mutations in two previously published families. RESULTS: In family 1, a missense mutation (c.965A-->T) causes a change of amino acid 322 from asparagine to isoleucine; this amino acid is located in a highly conserved motif likely to affect Ca2+ binding affecting specificity of the cell-cell binding function. In family 2, a homozygous frameshift deletion (c.829delG) introduces a truncated fusion protein with a premature stop codon at amino acid residue 295, expected to cause a non-functional protein lacking both its intracellular and membrane spanning domains and its extracellular cadherin repeats 3-5. Our mouse in situ expression data demonstrate that Cdh3 is expressed in the apical ectodermal ridge from E10.5 to E12.5, and later in the interdigital mesenchyme, a pattern compatible with the EEM phenotype. Furthermore, we discuss possible explanations for the phenotypic differences between EEM and congenital hypotrichosis with juvenile macular dystrophy (HJMD), which is also caused by CDH3 mutations. CONCLUSIONS: In summary, we have ascertained a third gene associated with ectrodactyly and have demonstrated a hitherto unrecognised role of CDH3 in shaping the human hand.
Asunto(s)
Cadherinas/genética , Distrofias Hereditarias de la Córnea/genética , Displasia Ectodérmica/genética , Mutación , Adulto , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Cadherinas/metabolismo , Niño , Homocigoto , Humanos , Hipotricosis/genética , Hibridación in Situ , Ratones , Modelos Genéticos , Datos de Secuencia Molecular , Linaje , Fenotipo , Alineación de Secuencia , SíndromeRESUMEN
The authors describe clinical, neuroimaging and molecular findings in a group of 15 patients with classic lissencephaly (LIS) and subcortical band heterotopia (SBH). A 1385A-->C mutation was found in the LIS1 gene in one patient with LIS more severe than expected for individuals with missense mutations in LIS1. The authors believe that the site of the mutation, present in a functionally critical region of the protein, could explain the unusual severe phenotype found in this patient.
Asunto(s)
Corteza Cerebral/anomalías , Proteínas Asociadas a Microtúbulos/genética , Malformaciones del Sistema Nervioso/genética , 1-Alquil-2-acetilglicerofosfocolina Esterasa , Adolescente , Adulto , Niño , Preescolar , Estudios de Cohortes , Análisis Mutacional de ADN , Femenino , Humanos , Lactante , Masculino , Mutación Missense , Malformaciones del Sistema Nervioso/patología , FenotipoRESUMEN
We report a male infant with an association of hypothyroidism and unusual facies, including blepharophimosis, which is similar to the dysmorphic features observed in the condition first described by Young and Simpson [(1987) J Med Genet 24:715-7161. On the other hand, the patient also shares many features with those reported as having Ohdo blepharophimosis syndrome [Ohdo et al, (1986) J Med Genet 23:242-244]. Previous case reports are reviewed and difficulties concerning the differential diagnosis of these conditions are discussed.
Asunto(s)
Anomalías Múltiples/diagnóstico , Blefarofimosis/patología , Hipotiroidismo/patología , Discapacidad Intelectual/patología , Anomalías Múltiples/patología , Diagnóstico Diferencial , Humanos , Lactante , Masculino , SíndromeRESUMEN
Investigation of the origin of sexual ambiguity is complex. Although testicular function has traditionally been assessed only by examining the steroidogenic capacity of Leydig cells and spermatogenesis, it has recently been shown that the measurement of serum anti-Müllerian hormone (AMH) as a marker of Sertoli cell function may also help clinicians. The aim of this study was to evaluate both Leydig and Sertoli cell functions in 46,XY patients with intersex states in order to establish biochemical patterns that would help to reach an etiologic diagnosis. We measured serum androgens, AMH and gonadotropins in 24 patients with sexual ambiguity and XY karyotype: 8 with gonadal dysgenesis (GD), 3 with 3beta-hydroxysteroid dehydrogenase deficiency (3betaHSD), 5 with androgen insensitivity syndrome (AIS), 4 with 5alpha-reductase 2 (SRD5A2) deficiency, and 4 were of unknown origin or idiopathic. Our results showed that while testosterone was low and gonadotropins elevated in patients with either GD or 3betaHSD, AMH was low in the former and high in the latter. Serum AMH and gonadotropins were normal or high in patients with 3betaHSD or AIS, but these could be distinguished by testosterone levels. Serum testosterone and gonadotropins were normal or high in AIS and SRD5A2 deficiency patients; however, while AMH was elevated in AIS, it was not the case in SRD5A2 deficiency patients, indicating that testosterone is sufficient to inhibit AMH within the testis. In idiopathic cases gonadotropins and testosterone were normal, and AMH was normal or low. We conclude that the combined measurement of androgens, AMH and gonadotropins helps to establish the diagnosis in intersex patients.
Asunto(s)
Trastornos del Desarrollo Sexual/fisiopatología , Glicoproteínas , Testículo/fisiopatología , 3-Hidroxiesteroide Deshidrogenasas/deficiencia , 3-Oxo-5-alfa-Esteroide 4-Deshidrogenasa/deficiencia , Adolescente , Síndrome de Resistencia Androgénica/fisiopatología , Hormona Antimülleriana , Niño , Preescolar , Gonadotropina Coriónica/farmacología , Hormona Folículo Estimulante/sangre , Disgenesia Gonadal/fisiopatología , Inhibidores de Crecimiento/sangre , Humanos , Lactante , Cariotipificación , Células Intersticiales del Testículo/fisiología , Hormona Luteinizante/sangre , Masculino , Células de Sertoli/fisiología , Hormonas Testiculares/sangre , Testosterona/sangreRESUMEN
We describe a woman with Ullrich-Turner manifestations and a 45,X/46, X,+mar karyotype. Fluorescence in situ hybridization (FISH) and DNA analysis were carried out in order to determine the origin and structure of the marker. FISH showed that the marker was a Y-derived dicentric chromosome. The breakpoint at Yq11 (interval 6) was mapped using Southern blotting and polymerase chain reaction (PCR). There were no nucleotide alterations in the SRY conserved domain. Histological analysis of the gonads showed an ovarian-like stroma with no signs of testicular tissue. These findings indicate that the patient was a mosaic 45,X/46,X,idic(Yp) whose phenotypic expression, including sex determination, appeared to have had more influence from the 45,X cell line.
Asunto(s)
Isocromosomas , Síndrome de Turner/genética , Cromosoma Y , Adulto , Southern Blotting , Bandeo Cromosómico , Femenino , Marcadores Genéticos , Humanos , Hibridación Fluorescente in Situ , Cariotipificación , Masculino , Modelos Genéticos , Reacción en Cadena de la Polimerasa , Lugares Marcados de SecuenciaRESUMEN
We report on three sibs presenting with spondylocarpotarsal synostosis, short-trunk dwarfism of postnatal onset, scoliosis, unsegmented thoracic vertebrae with unilateral bar, and carpal bone fusion. Tarsal bone fusion and dental abnormalities were noted in some of them, indicating pleiotropy and intrafamilial variability. Lens opacities, rarefaction of retinal pigmentation, and narrowing of retinal vessels, detected in two patients, are findings that have not been described to date in this condition.
Asunto(s)
Huesos del Carpo/anomalías , Anomalías del Ojo/diagnóstico , Columna Vertebral/anomalías , Sinostosis/diagnóstico , Huesos Tarsianos/anomalías , Anomalías Múltiples/diagnóstico , Adolescente , Adulto , Huesos del Carpo/diagnóstico por imagen , Bandeo Cromosómico , Enanismo/diagnóstico , Salud de la Familia , Femenino , Humanos , Masculino , Linaje , Radiografía , Columna Vertebral/diagnóstico por imagen , Huesos Tarsianos/diagnóstico por imagenRESUMEN
We report on a Brazilian kindred in which two sibs presented with the complete form of EEM (ectodermal dysplasia, ectrodactyly, and macular dystrophy) syndrome with hypotrichosis, dental anomalies, syndactyly, and retinal changes with prominent pigmentation in the posterior pole of the retina. In this family, we also observed another sib with syndactyly, as well as a first cousin with ectrodactyly. A 10-year follow-up demonstrated gradually decreasing visual acuity and progression of retinal degenerative anomalies.
Asunto(s)
Displasia Ectodérmica/genética , Deformidades Congénitas de la Mano/genética , Degeneración Macular/genética , Adulto , Angiografía con Fluoresceína , Estudios de Seguimiento , Humanos , Hipotricosis/genética , Degeneración Macular/fisiopatología , Masculino , Linaje , Retina/anomalías , Retina/patología , Síndrome , Anomalías Dentarias/genéticaRESUMEN
Sex ambiguity may be due to several disorders of gonadal differentiation, including true hermaphroditism (TH), as well as male and female pseudohermaphroditism. Although TH is a rare cause of intersex in Europe and North America, in Africa it presents one of the highest frequencies. The 46,XX karyotype has been found in the majority of the reported patients (70.6%), and aberrations in the sex chromosomes have been observed in about 22% of the cases. The 46,XY karyotype has been described as less frequent. Herein we describe ten cases of TH which have been diagnosed over the last 7 years, six lateral TH, two unilateral TH, and two cases of ovotestes with absent contralateral gonad. From a total of 18 gonads analyzed, there were 8 testes, 6 ovaries and 4 ovotestes. Nine subjects had originally a male sex assignment, and in three cases this was reverted to female. Four cases had a 46,XY karyotype. Additional sex chromosome aberrations had been found in four different cases [two 46,XX/46,XY, one 45,X/47,XYY, one 46,X,del(Yq)]. A 46,XX karyotype was found in only two individuals, and both were SRY negative. Our preliminary data, especially on the constitution of chromosomes and gonads, indicate marked differences from those in the literature.
Asunto(s)
Trastornos del Desarrollo Sexual/genética , Ovario/anomalías , Testículo/anomalías , Adolescente , Brasil , Diferenciación Celular/fisiología , Niño , Preescolar , Trastornos del Desarrollo Sexual/patología , Femenino , Humanos , Lactante , Cariotipificación , Masculino , Estudios RetrospectivosRESUMEN
We studied 11 patients (9 males) with cytogenetic diagnosis of fragile X syndrome (FXS) with the purpose of investigating the neural circuitry involved in this condition. The ages ranged from 8 to 19. All the individuals presented large ears, elongated faces and autistic features. Ten patients had severe mental retardation. Attention disorder was found in 10 individuals. Electroencephalographic recordings were abnormal in 6 of 10 patients examined, showing focal epileptiform discharges predominantly in frontal and parietal areas. All patients underwent magnetic resonance imaging studies which were abnormal in 8 of them. The most important abnormalities were reduction of the cerebellar vermis and enlargement of the IV ventricle. Single photon emission computerized tomography (SPECT) was performed in 7 patients and was abnormal in all of them, the most frequent finding being a hypoperfusion of the inferior of the frontal lobes. Based on the clinical picture, neuropsychological findings and functional and structural imaging studies we suggest that FXS presents with a dysfunction involving a large area of the central nervous system: cerebellum-basal frontal regions-parietal lobes. The literature points to a disturbance involving the same neural circuitry in patients with autism.
Asunto(s)
Síndrome del Cromosoma X Frágil/diagnóstico , Adolescente , Adulto , Encéfalo/patología , Niño , Electroencefalografía , Femenino , Síndrome del Cromosoma X Frágil/psicología , Humanos , Imagen por Resonancia Magnética , Masculino , Examen Neurológico , Pruebas Neuropsicológicas , Tomografía Computarizada de Emisión de Fotón ÚnicoRESUMEN
We report on a rare case of female pseudohermaphroditism due to classical 21-hydroxylase deficiency associated with Turner syndrome (45,X/46,XX). Difficulties in the management of both diseases are briefly discussed. We regard this rare combination as a coincidental occurrence.
Asunto(s)
Hiperplasia Suprarrenal Congénita/genética , Trastornos del Desarrollo Sexual/genética , Esteroide 21-Hidroxilasa/genética , Síndrome de Turner/genética , Trastornos del Desarrollo Sexual/complicaciones , Trastornos del Desarrollo Sexual/enzimología , Trastornos del Desarrollo Sexual/terapia , Femenino , Humanos , Lactante , Síndrome de Turner/complicaciones , Síndrome de Turner/enzimología , Síndrome de Turner/terapiaRESUMEN
We have studied a boy with a particular clinical picture of mental retardation, hypotrichosis, early eruption of teeth, and syndactyly of hands. One sister, who died at four month of age, probably was also affected. This clinical association may represent an undescribed condition. Autosomal recessive inheritance is suggested.
Asunto(s)
Hipotricosis/genética , Discapacidad Intelectual/genética , Sindactilia/genética , Preescolar , Diagnóstico Diferencial , Displasia Ectodérmica/diagnóstico , Displasia Ectodérmica/genética , Genes Recesivos , Humanos , Hipotricosis/diagnóstico , Discapacidad Intelectual/diagnóstico , Masculino , Fenotipo , Sindactilia/diagnóstico , Síndrome , Anomalías Dentarias/diagnóstico , Anomalías Dentarias/genéticaRESUMEN
We describe a four-generation Brazilian family with short tarsus and absence of the lower eyelashes, with normal intelligence. Autosomal dominant inheritance is evident.
Asunto(s)
Tobillo/anomalías , Aberraciones Cromosómicas , Trastornos de los Cromosomas , Pestañas/anomalías , Adolescente , Brasil , Femenino , Humanos , Masculino , LinajeRESUMEN
We report on a 5-year-old girl with a male karyotype (46,XY), severe psychomotor and physical retardation, minor anomalies, and female external genitalia with a blindly ending vagina. She has normal adrenal function, prepubertal serum gonadotropin and testosterone levels, which did not rise after hCG stimulation. On abdominal exploration no gonads were found, and only mesonephric and Müllerian remnants. She was HY positive, and no deletion was detected in the Y chromosome using 5 different probes. Although a genetic defect is not excluded, pregnancy complications suggest an environmental insult to the developing testes.
Asunto(s)
Testículo/anomalías , Preescolar , Sondas de ADN , Trastornos del Desarrollo Sexual/genética , Genitales/anomalías , Humanos , Masculino , Fenotipo , Cromosoma YRESUMEN
We report a dup(12p) due to a de novo i(12p) in a girl with mosaicism for 12q whole-arm translocations onto 7p, 7q, and 11q terminal regions. The dup(12p) syndrome was confirmed by clinical, cytogenetic, and LDH-dosage studies.