Müllerian anomalies, hearing loss, and connexin 26 mutations

Fertil Steril. 2006 Jun;85(6):1824-5. doi: 10.1016/j.fertnstert.2005.11.050. Epub 2006 May 2.

Abstract

In a study of the possible inter-relationship among müllerian anomalies, hearing loss, and connexin 26 mutations, we evaluated all women in whom müllerian anomalies were diagnosed on hysterosalpingography during a 6-year period (n = 24/519). Audiometric testing revealed five (22.7%) with unrecognized sensorineural hearing loss; however, on genetic evaluation, none harbored a connexin 26 mutation.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Connexin 26
  • Connexins / genetics*
  • Female
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Hearing Loss, Sensorineural / diagnosis
  • Hearing Loss, Sensorineural / epidemiology*
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Mullerian Ducts / abnormalities*
  • Prevalence
  • Retrospective Studies
  • Risk Assessment / methods*
  • Risk Factors

Substances

  • Connexins
  • Connexin 26