A 47,XXY Pregnant Woman without the SRY Gene

Sex Dev. 2019;13(2):83-86. doi: 10.1159/000496996. Epub 2019 Feb 16.

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.

Keywords: 47,XXY; SRY; Y chromosome.

Publication types

  • Case Reports

MeSH terms

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

Substances

  • SRY protein, human
  • Sex-Determining Region Y Protein