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Sex Dev ; 13(2): 83-86, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30799415

RESUMO

Individuals with a 47,XXY karyotype usually present with a male phenotype due to the additional Y chromosome. In this paper, we describe a 47,XXY female who was pregnant with a fetus of the same karyotype based on chromosome analysis of amniotic fluid cells. Further analysis of her Y chromosome indicated that the additional Y chromosome contains no SRY gene on the short arm but carries the azoospermia factor region on the long arm, including azoospermia factor a, b and c (AZFa, AZFb, AZFc). This region may influence her female phenotype. Fertile females with a 47,XXY karyotype and loss of SRY are extremely rare. This paper is the first report of a 47,XXY pregnant woman with a normal phenotype and may enrich our knowledge on 47,XXY individuals.


Assuntos
Cromossomos Humanos X/genética , Cromossomos Humanos Y/genética , Transtornos dos Cromossomos Sexuais/genética , Proteína da Região Y Determinante do Sexo/genética , Adulto , Bandeamento Cromossômico , Deleção Cromossômica , Feminino , Humanos , Cariotipagem , Masculino , Linhagem , Gravidez , Transtornos dos Cromossomos Sexuais/sangue , Proteína da Região Y Determinante do Sexo/metabolismo
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