Cochlear Nerve Canal Stenosis: Association With MYH14 and MYH9 Genes

Author:

Liang Wenqi1,Wang Line1,Song Xinyu1,Gao Fenqi1,Liu Pan1,Lee Tiffany H.2,Peng Kevin A.3ORCID

Affiliation:

1. Department of Otorhinolaryngology–Head and Neck Surgery, Beijing Friendship Hospital, Capital Medical University, Beijing, People’s Republic of China

2. LAC+USC Medical Center , Los Angeles, CA, USA

3. House Clinic and House Ear Institute, Los Angeles, CA, USA

Abstract

The bony cochlear nerve canal transmits the cochlear nerve as it passes from the fundus of the internal auditory canal to the cochlea. Stenosis of the cochlear nerve canal, defined as a diameter less than 1.0 mm in transverse diameter, is associated with inner ear anomalies and severe to profound congenital hearing loss. We describe an 11-month-old infant with nonsyndromic congenital sensorineural hearing loss with cochlear nerve canal stenosis. Next-generation sequencing revealed heterozygous mutations in MYH9 and MYH14, encoding for the inner ear proteins myosin heavy chain IIA and IIC. The patient’s hearing was rehabilitated with bilateral cochlear implantation.

Publisher

SAGE Publications

Subject

Otorhinolaryngology

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