Müllerian anomalies, hearing loss, and connexin 26 mutations

Jacob Rabinson, Raoul Orvieto*, Amnon Shapira, Zippora Brownstein, Simion Meltzer, Ilan Tur-Kaspa

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review


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.

Original languageEnglish
Pages (from-to)1824-1825
Number of pages2
JournalFertility and Sterility
Issue number6
StatePublished - Jun 2006
Externally publishedYes


Dive into the research topics of 'Müllerian anomalies, hearing loss, and connexin 26 mutations'. Together they form a unique fingerprint.

Cite this