Chromosomal abnormalities in women with premature ovarian failure

Gynecol Endocrinol. 2010 Oct;26(10):717-24. doi: 10.3109/09513590.2010.500427.

Abstract

Premature ovarian failure is a complex disorder that results in the early loss of ovarian function; however this disease must be separated from early menopause because these patients can sporadically ovulate and in literature are described pregnancies. The aetiology and the patho-physiology of premature ovarian failure are still matter of debate, but is commonly accepted that genetic factors play an important role. This review is aimed to present an overview of known inherited factor implied in the pathogenesis of this disorder to help physician in the counselling of affected pregnant women.

Publication types

  • Review

MeSH terms

  • Chromosome Aberrations*
  • Chromosome Disorders / complications*
  • Chromosomes, Human, X*
  • Female
  • Humans
  • Inhibins / genetics
  • Membrane Proteins / genetics
  • Mutation
  • Primary Ovarian Insufficiency / genetics*
  • Receptors, FSH / genetics
  • Receptors, LH / genetics
  • Receptors, Progesterone / genetics

Substances

  • Membrane Proteins
  • PGRMC1 protein, human
  • Receptors, FSH
  • Receptors, LH
  • Receptors, Progesterone
  • inhibin-alpha subunit
  • Inhibins