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Sex Dev ; 13(2): 83-86, 2019.
Article in English | MEDLINE | ID: mdl-30799415

ABSTRACT

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.


Subject(s)
Chromosomes, Human, X/genetics , Chromosomes, Human, Y/genetics , Sex Chromosome Disorders/genetics , Sex-Determining Region Y Protein/genetics , Adult , Chromosome Banding , Chromosome Deletion , Female , Humans , Karyotyping , Male , Pedigree , Pregnancy , Sex Chromosome Disorders/blood , Sex-Determining Region Y Protein/metabolism
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