Ovaries and female phenotype in a girl with 46,XY karyotype and mutations in the CBX2 gene.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 19361780.
- Also identified by DOI 10.1016/j.ajhg.2009.03.016 and PMC identifier 2680992.
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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.
Medical subject headings
- Gonadal Dysgenesis, 46,XY
- Ovary
- Repressor Proteins