Literature DB >> 11556849

Connexin 26 studies in patients with sensorineural hearing loss.

M A Kenna1, B L Wu, D A Cotanche, B R Korf, H L Rehm.   

Abstract

OBJECTIVE: To determine the spectrum of connexin 26 (Cx26) mutations and their phenotypes in children with sensorineural hearing loss (SNHL) or mixed hearing loss (MHL).
DESIGN: Children with SNHL or MHL were prospectively tested for mutations in the entire coding region of the Cx26 gene. PATIENTS: Children with SNHL or MHL with no obvious etiology for the hearing loss.
RESULTS: Between December 1, 1998, and July 1, 2000, 107 patients with SNHL or MHL from 99 families underwent Cx26 testing. Most patients were aged 1 week to 16 years (61 boys and 46 girls). Thirty (30%) of 99 probands had Cx26 mutations: biallelic mutations were detected in 18 (9 homozygous and 9 compound heterozygous) and single mutations were detected in 12. Twelve previously reported mutations (35delG, 167delT, E47X, L90P, M34T, G12V, V37I, R143W, V84L, V153I, V27I, and 310del14) and 3 novel mutations (E129K, T8M, and N206S) were found. Hearing loss in patients with biallelic Cx26 mutations ranged from unilateral high frequency to bilateral profound. Four children, 2 with biallelic mutations, had temporal bone abnormalities.
CONCLUSIONS: Connexin 26 mutations are common in children with SNHL, and it is likely that the homozygous and compound heterozygous mutations cause the SNHL. However, pathogenicity is less certain when only a single Cx26 mutation is present. Patients with biallelic Cx26 mutations had a slightly higher incidence of milder hearing loss than in previous studies. Children with SNHL or MHL should be tested for Cx26 mutations early in their evaluation.

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Year:  2001        PMID: 11556849     DOI: 10.1001/archotol.127.9.1037

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


  31 in total

1.  Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece.

Authors:  V Iliadou; N Eleftheriades; A S Metaxas; A Skevas; T Kiratzidis; A Pampanos; N Voyiatzis; M Grigoriadou; M B Petersen; T Iliades
Journal:  Eur Arch Otorhinolaryngol       Date:  2003-09-30       Impact factor: 2.503

2.  Deaf adults' reasons for genetic testing depend on cultural affiliation: results from a prospective, longitudinal genetic counseling and testing study.

Authors:  Patrick Boudreault; Erin E Baldwin; Michelle Fox; Loriel Dutton; Leeelle Tullis; Joyce Linden; Yoko Kobayashi; Jin Zhou; Janet S Sinsheimer; Yvonne Sininger; Wayne W Grody; Christina G S Palmer
Journal:  J Deaf Stud Deaf Educ       Date:  2010-05-20

3.  DNA sequence analysis of GJB2, encoding connexin 26: observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls.

Authors:  Hsiao-Yuan Tang; Ping Fang; Patricia A Ward; Eric Schmitt; Sandra Darilek; Spiros Manolidis; John S Oghalai; Benjamin B Roa; Raye Lynn Alford
Journal:  Am J Med Genet A       Date:  2006-11-15       Impact factor: 2.802

4.  Calcium interactions with Cx26 hemmichannel: Spatial association between MD simulations biding sites and variant pathogenicity.

Authors:  Juan M R Albano; Nahuel Mussini; Roxana Toriano; Julio C Facelli; Marta B Ferraro; Mónica Pickholz
Journal:  Comput Biol Chem       Date:  2018-11-12       Impact factor: 2.877

Review 5.  Do cell junction protein mutations cause an airway phenotype in mice or humans?

Authors:  Eugene H Chang; Alejandro A Pezzulo; Joseph Zabner
Journal:  Am J Respir Cell Mol Biol       Date:  2011-02-04       Impact factor: 6.914

6.  Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations.

Authors:  Kenneth H Lee; Daniel A Larson; Gordon Shott; Brian Rasmussen; Aliza P Cohen; Corning Benton; Mark Halsted; Daniel Choo; Jareen Meinzen-Derr; John H Greinwald
Journal:  Laryngoscope       Date:  2009-03       Impact factor: 3.325

7.  Audiologic phenotype and progression in GJB2 (Connexin 26) hearing loss.

Authors:  Margaret A Kenna; Henry A Feldman; Marilyn W Neault; Anna Frangulov; Bai-Lin Wu; Brian Fligor; Heidi L Rehm
Journal:  Arch Otolaryngol Head Neck Surg       Date:  2010-01

8.  Altered gating properties of functional Cx26 mutants associated with recessive non-syndromic hearing loss.

Authors:  Gülistan Meşe; Eric Londin; Rickie Mui; Peter R Brink; Thomas W White
Journal:  Hum Genet       Date:  2004-07-07       Impact factor: 4.132

Review 9.  Causation of permanent unilateral and mild bilateral hearing loss in children.

Authors:  Anne Marie Tharpe; Douglas P Sladen
Journal:  Trends Amplif       Date:  2008-03

Review 10.  Congenital hearing impairment.

Authors:  Caroline D Robson
Journal:  Pediatr Radiol       Date:  2006-02-08
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