Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family.

Autosomal Recessive Congenital Sensorineural Hearing Loss due to a Novel Compound Heterozygous PTPRQ Mutation in a Chinese Family.
Neural Plast. 2018;2018:9425725
Authors: Wu X, Wang S, Chen S, Wen YY, Liu B, Xie W, Li D, Liu L, Huang X, Sun Y, Kong WJ
Abstract
PTPRQ gene, encoding protein tyrosine phosphatase receptor Q, is essential for the normal maturation and function of hair bundle in the cochlea. Its mutations can cause the defects of stereocilia in hair cell, which lead to nonsyndromic sensorineural hearing loss. Using next-generation sequencing and Sanger sequencing method, we identified a novel compound heterozygous missense mutation, c.4472C>T p.T1491M (maternal allele) and c.1973T>C p.V658A (paternal allele), in PTPRQ gene. The two mutations are the first reported to be the cause of recessively inherited sensorineural hearing loss. Hearing loss levels and progression involved by PTPRQ mutations among the existing cases seem to be varied, and the relationship between genotypes and phenotypes is unclear. Our data here further prove the important role of PTPRQ in auditory function and provide more information for the further mechanism research of PTPRQ-related hearing loss.
PMID: 29849575 [PubMed - in process]

Source: Neural Plasticity - June 6, 2018 Category: Neurology Authors: Wu X, Wang S, Chen S, Wen YY, Liu B, Xie W, Li D, Liu L, Huang X, Sun Y, Kong WJ Tags: Neural Plast Source Type: research