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Article

Molecular analysis in diagnostic procedure of hearing impairment in newborns.

Croatian medical journal - 1 Oct 2005

Zaputovic Sanja, Stimac Tea, Prpic Igor, Mahulja-Stamenkovic Vesna, Medica Igor, Peterlin Borut

Abstract excerpt

AIM: To determine the proportion of newborns diagnosed with hearing impairment through the hearing impairment screening program in newborns, and the frequency of 35delG/GJB2 mutation as a cause of hearing impairment. The results of the study imply the integration of the mutation analysis in the neonatal screening program. METHODS: Evoked otoacustic emission (E-OAE) screening program was performed among 6019...

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Identifiers

PMID: 16158474

Genes

GJB2

Provenance

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