Research Article

Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss

Table 1

The clinical information of the patients.

Proband numberAgeGenderAge onsetHearing impairmentABRDPOAETympanogramMRI/CT

12 yrF0Profound85 dBAbsentAs(L)/A(R)Normal
21 yrM0Profound105 dBAbsentA(L)/A(R)Normal

ABR: auditory brainstem response; DPOAE: distortion product otoacoustic emissions; A: A type; As: As type.