1. Academic Validation
  2. Ovaries and female phenotype in a girl with 46,XY karyotype and mutations in the CBX2 gene

Ovaries and female phenotype in a girl with 46,XY karyotype and mutations in the CBX2 gene

  • Am J Hum Genet. 2009 May;84(5):658-63. doi: 10.1016/j.ajhg.2009.03.016.
Anna Biason-Lauber 1 Daniel Konrad Monika Meyer Carine DeBeaufort Eugen J Schoenle
Affiliations

Affiliation

  • 1 Division of Endocrinology/Diabetology, University Children's Hospital, 8032 Zurich, Switzerland. anna.lauber@kispi.uzh.ch
Abstract

A girl with a prenatal 46,XY karyotype was born with a completely normal female phenotype, including uterus and histologically normal ovaries. In mice with a similar phenotype, the ablation of M33, an ortholog of Drosophila Polycomb, causes male-to-female sex reversal. The analysis of the human homolog of M33, Chromobox homolog 2 (CBX2), in this girl revealed loss-of-function mutations that allowed us, by placing CBX2 upstream of SRY, to add an additional component to the still incomplete cascade of human sex development.

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