Literature DB >> 11556850

Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH.

S J Bom1, E M De Leenheer, F X Lemaire, M H Kemperman, W I Verhagen, H A Marres, H P Kunst, R J Ensink, A J Bosman, G Van Camp, F P Cremers, P L Huygen, C W Cremers.   

Abstract

OBJECTIVE: To analyze the relationship between pure-tone hearing threshold and speech recognition performance in DFNA2/KCNQ4 and DFNA9/COCH, 2 types of high-frequency nonsyndromic hearing impairment.
DESIGN: Case series with cross-sectional analysis of phoneme recognition scores related to age and hearing level.
SETTING: University hospital. PATIENTS: Forty-five members of 4 separate families, all carrying 1 of 3 different mutations in the KCNQ4 gene at the DFNA2 locus (1p34); 42 members of 7 separate families, all carrying the same Pro51Ser mutation in the COCH gene at the DFNA9 locus (14q12-q13).
RESULTS: The deterioration of speech recognition dropped to a 90% score at a higher level of hearing impairment (pure-tone-average at 1, 2, and 4 kHz) in DFNA2-affected patients (65 dB) than in DFNA9-affected patients (46 dB).
CONCLUSION: At similar levels of hearing impairment, DFNA2/KCNQ4-affected patients showed better speech recognition performance than DFNA9/COCH-affected patients.

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Year:  2001        PMID: 11556850     DOI: 10.1001/archotol.127.9.1045

Source DB:  PubMed          Journal:  Arch Otolaryngol Head Neck Surg        ISSN: 0886-4470


  5 in total

1.  A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation.

Authors:  Rutger F Plantinga; Arjan P M de Brouwer; Patrick L M Huygen; Henricus P M Kunst; Hannie Kremer; Cor W R J Cremers
Journal:  J Assoc Res Otolaryngol       Date:  2006-04-25

2.  Molecular biology of hearing.

Authors:  Timo Stöver; Marc Diensthuber
Journal:  GMS Curr Top Otorhinolaryngol Head Neck Surg       Date:  2012-04-26

3.  Genotype-phenotype correlation in DFNB8/10 families with TMPRSS3 mutations.

Authors:  Nicole J D Weegerink; Margit Schraders; Jaap Oostrik; Patrick L M Huygen; Tim M Strom; Susanne Granneman; Ronald J E Pennings; Hanka Venselaar; Lies H Hoefsloot; Mariet Elting; Cor W R J Cremers; Ronald J C Admiraal; Hannie Kremer; Henricus P M Kunst
Journal:  J Assoc Res Otolaryngol       Date:  2011-07-23

Review 4.  Genotype-Phenotype Correlations of Pathogenic COCH Variants in DFNA9: A HuGE Systematic Review and Audiometric Meta-Analysis.

Authors:  Sybren M M Robijn; Jeroen J Smits; Kadriye Sezer; Patrick L M Huygen; Andy J Beynon; Erwin van Wijk; Hannie Kremer; Erik de Vrieze; Cornelis P Lanting; Ronald J E Pennings
Journal:  Biomolecules       Date:  2022-01-27

5.  Genotype-phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9): Part I-A Cross-sectional Study of Hearing Function in 111 Carriers.

Authors:  Sebastien P F JanssensdeVarebeke; Julie Moyaert; Erik Fransen; Britt Bulen; Celine Neesen; Katrien Devroye; Raymond van de Berg; Ronald J E Pennings; Vedat Topsakal; Olivier Vanderveken; Guy Van Camp; Vincent Van Rompaey
Journal:  Ear Hear       Date:  2021 Nov-Dec 01       Impact factor: 3.570

  5 in total

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