Ontology highlight
ABSTRACT:
SUBMITTER: Thorpe RK
PROVIDER: S-EPMC9092196 | biostudies-literature | 2022 Apr
REPOSITORIES: biostudies-literature
Thorpe Ryan K RK Walls W Daniel WD Corrigan Rae R Schaefer Amanda A Wang Kai K Huygen Patrick P Casavant Thomas L TL Smith Richard J H RJH
Human genetics 20220117 3-4
Autosomal dominant non-syndromic hearing loss (ADNSHL) displays gene-specific progression of hearing loss, which is amenable to sequential audioprofiling. We sought to refine the natural history of ADNSHL by examining audiometric data in 5-year increments. 2175 audiograms were included from four genetic causes of ADNSHL-KCNQ4 (DFNA2), GSDME (DFNA5), WFS1 (DFNA6/14/38), and COCH (DFNA9). Annual threshold deterioration (ATD) was calculated for each gene: for the speech-frequency pure tone average, ...[more]