Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing Impairment. Issue 1 (January 2016)

• Record Type: Journal Article
• Authors: van Beelen, Eline; Oonk, Anne M. M.; Leijendeckers, Joop M.; Hoefsloot, Elisabeth H.; Pennings, Ronald J. E.; Feenstra, Ilse; Dieker, Hendrik-Jan; Huygen, Patrick L. M.; Snik, Ad F. M.; Kremer, Hannie; Kunst, Henricus P. M.
• Is Part Of: Ear and hearing. Volume 37:Issue 1(2016:Jan./Feb.)
• Publication Date: 2016-01
• Subjects: DFNA10 -- EYA4 -- Hearing impairment -- Sensory type; Hearing disorders -- Periodicals; Audiology -- Periodicals; 612.85
• DOI: 10.1097/AUD.0000000000000217
• Languages: English
• ISSNs: 0196-0202

Abstract

Abstract : Objectives: Mutations in EYA4 can cause nonsyndromic autosomal dominant sensorineural hearing impairment (DFNA10) or a syndromic variant with hearing impairment and dilated cardiomyopathy. A mutation in EYA4 was found in a Dutch family, causing DFNA10. This study is focused on characterizing the hearing impairment in this family. Design: Whole exome sequencing was performed in the proband. In addition, peripheral blood samples were collected from 23 family members, and segregation analyses were performed. All participants underwent otorhinolaryngological examinations and pure-tone audiometry, and 12 participants underwent speech audiometry. In addition, an extended set of audiometric measurements was performed in five family members to evaluate the functional status of the cochlea. Vestibular testing was performed in three family members. Two individuals underwent echocardiography to evaluate the nonsyndromic phenotype. Results: The authors present a Dutch family with a truncating mutation in EYA4 causing a mid-frequency hearing impairment. This mutation (c.464del) leads to a frameshift and a premature stop codon (p.Pro155fsX). This mutation is the most N-terminal mutation in EYA4 found to date. In addition, a missense mutation, predicted to be deleterious, was found in EYA4 in two family members. Echocardiography in two family members revealed no signs of dilated cardiomyopathy. Results of caloric and velocity step tests in three family members showed no abnormalities. Hearing impairment was found to be symmetric and progressive, beginning as a mid-frequency hearing impairment in childhood and developing into a high-frequency, moderate hearing impairment later in life. Furthermore, an extended set of audiometric measurements was performed in five family members. The results were comparable to those obtained in patients with other sensory types of hearing impairments, such as patients with Usher syndrome type IIA and presbyacusis, and not to those obtained in patients with (cochlear) conductive types of hearing impairment, such as DFNA8/12 and DFNA13. Conclusions: The mid-frequency hearing impairment in the present family was found to be symmetric and progressive, with a predominantly childhood onset. The results of psychophysical measurements revealed similarities to other conditions involving a sensory type of hearing impairment, such as Usher syndrome type IIA and presbyacusis. The study results suggest that EYA4 is expressed in the sensory cells of the cochlea. This phenotypic description will facilitate counseling for hearing impairment in DFNA10 patients. Abstract : We present a Dutch family with a mutation in EYA4 causing DFNA10. This study focused on characterizing the hearing impairment in this family. Mutations in EYA4 can cause DFNA10 or a syndromic variant with hearing impairment and dilated cardiomyopathy. Echocardiography in this family revealed no signs of dilated cardiomyopathy. Hearing impairment was found to be mid-frequency, symmetric, and progressive, with a predominantly childhood onset. Additionally, the results of an extended set of audiometric measurements were comparable to those obtained with other hearing impairments of the sensory type. Our results suggest that EYA4 is expressed in sensory cells of the cochlea.