Case report: Compound heterozygous nonsense PCDH15 variant and a novel deep‐intronic variant in a Chinese child with profound hearing loss

Author:

Yang Ziying12ORCID,Huang Minhong3,Wei Xiuxiu2,Sun Jun2,Zhang Fuping3

Affiliation:

1. College of Life Sciences University of Chinese Academy of Sciences Beijing China

2. Tianjin Medical Laboratory, BGI‐Tianjin, BGI‐Shenzhen Tianjin China

3. Unicare Clinic, BGI Genomics Co., Ltd., BGI‐Shenzhen Shenzhen China

Abstract

AbstractBackgroundUsher syndrome is a condition characterized by partial or total hearing loss and progressive pigmentary retinopathy. Usher syndrome type 1F is caused by biallelic loss‐of‐function variants in Protocadherin 15 (PCDH15), which encodes the PCDH15 protein that plays an important role in the morphogenesis and cohesion of stereocilium bundles and retinal photoreceptor cell maintenance and function.MethodsWe report a child with bilateral nonsyndromic sensorineural hearing loss who received an inconclusive diagnosis based on clinical gene panel testing, which identified a paternal heterozygous nonsense variant (NM_033056.4: c.733C>T, p.R245*) in PCDH15. This variant has been described as a founder variant in the Ashkenazi Jewish population.ResultsA novel deep‐intronic variant (NM_033056.4: c.705+3767_705+3768del) inherited from the patient's mother was identified by trio‐based whole‐genome sequencing (WGS). A minigene splicing assay revealed that c.705+3767_705+3768del results in aberrant retention of 50 or 68 bp of intron 7.ConclusionOur genetic test results provided precise genetic counseling and prenatal diagnosis for this family, and our findings highlight the power of WGS for detecting deep‐intronic variants in patients with undiagnosed rare diseases. Additionally, this case expands the variant spectrum of the PCDH15 gene and our results support the extremely low carrier frequency of c.733C>T in the Chinese population.

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

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