Searching for the polycystic ovary syndrome genes

J Pediatr Endocrinol Metab. 2000:13 Suppl 5:1311-3.

Abstract

PCOS is a common disorder of unknown etiology. Studies of first-degree relatives of women diagnosed with PCOS suggest familial clustering of the disease. A prospective study of first-degree female relatives of women with PCOS conducted by NCPIR found that 46% of ascertainable sisters of women with PCOS were hyperandrogenemic. NCPIR has conducted linkage and association studies using affected sibling-pair analysis and the transmission/disequilibrium test to explore candidate PCOS genes. These studies point a finger at a region 1 MB centromeric to the insulin receptor gene on chromosome 19.

Publication types

  • Review

MeSH terms

  • Female
  • Genetic Linkage
  • Humans
  • Polycystic Ovary Syndrome / genetics*