Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Assunto da revista
País de afiliação
Intervalo de ano de publicação
1.
Am J Med Genet A ; 170(12): 3227-3230, 2016 12.
Artigo em Inglês | MEDLINE | ID: mdl-27500688

RESUMO

Maternal uniparental disomy of chromosome 6 [upd(6)mat] is rare and has only been previously reported 13 times with the main associated phenotype being IUGR. We present a case of a male patient with isodisomy upd(6)mat resulting in severe IUGR and ambiguous genitalia, a phenotype not previously described in association with this chromosome finding. The patient initially presented prenatally with IUGR at 19 weeks gestation with placental dysfunction and ambiguous genitalia noted at 27 weeks. Postnatally, the patient had external genital abnormalities, the gonads were in the inguinal canal and there was a rudimentary appearing vagina and uterus. Karyotype is 46, XY and SNP array revealed maternal isodisomy of 171 Mb at 6p25.3q27 with no pathogenic copy number variants. To our best knowledge, this is the first case of an XY patient with upd(6)mat with IUGR and ambiguous genitalia, further supporting previous reports regarding an association between upd(6)mat and IUGR. This patient also presented with a disorder of sex development (46, XY DSD) with the sex chromosome being male and positive for the SRY gene, testicular gonadal sex and abnormal external and internal genitalia. © 2016 Wiley Periodicals, Inc.


Assuntos
Cromossomos Humanos Par 6 , Transtornos do Desenvolvimento Sexual/genética , Retardo do Crescimento Fetal/genética , Ductos Paramesonéfricos/anormalidades , Fenótipo , Dissomia Uniparental , Transtornos do Desenvolvimento Sexual/diagnóstico , Retardo do Crescimento Fetal/diagnóstico , Estudos de Associação Genética , Humanos , Hibridização in Situ Fluorescente , Recém-Nascido , Cariótipo , Masculino , Exame Físico , Desenvolvimento Sexual/genética , Ultrassonografia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA