Literature DB >> 16885744

Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome.

Andrew J Griffith1, Yandan Yang, Shannon P Pryor, Hong-Joon Park, Ethylin Wang Jabs, Joseph B Nadol, Laura J Russell, Daniel I Wasserman, Gabriele Richard, Joe C Adams, Saumil N Merchant.   

Abstract

OBJECTIVE: The objective of this study was to characterize the temporal bone phenotype associated with a mutation of GJB2 (encoding connexin 26). STUDY
DESIGN: The authors conducted correlative clinical, molecular genetic, and postmortem histopathologic analysis.
METHODS: The study subject was a male infant with keratitis-ichthyosis-deafness (KID) syndrome. We performed a nucleotide sequence analysis of GJB2 and a histopathologic analysis of the temporal bones.
RESULTS: The subject was heterozygous for G45E, a previously reported KID syndrome mutation of GJB2. The primary inner ear abnormality was dysplasia of the cochlear and saccular neuroepithelium.
CONCLUSIONS: GJB2 mutations can cause deafness in KID syndrome, and possibly in other GJB2 mutant phenotypes, by disrupting cochlear differentiation.

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Year:  2006        PMID: 16885744      PMCID: PMC2563154          DOI: 10.1097/01.mlg.0000224549.75161.ca

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  14 in total

1.  A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.

Authors:  Ignacio del Castillo; Manuela Villamar; Miguel A Moreno-Pelayo; Francisco J del Castillo; Araceli Alvarez; Dolores Tellería; Ibis Menéndez; Felipe Moreno
Journal:  N Engl J Med       Date:  2002-01-24       Impact factor: 91.245

2.  Temporal bone histopathology in connexin 26-related hearing loss.

Authors:  A I Jun; W T McGuirt; R Hinojosa; G E Green; N Fischel-Ghodsian; R J Smith
Journal:  Laryngoscope       Date:  2000-02       Impact factor: 3.325

3.  Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome.

Authors:  Yvonne M Szymko-Bennett; Laura J Russell; Sherri J Bale; Andrew J Griffith
Journal:  Laryngoscope       Date:  2002-02       Impact factor: 3.325

4.  Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.

Authors:  Gabriele Richard; Fatima Rouan; Colin E Willoughby; Nkecha Brown; Pil Chung; Markku Ryynänen; Ethylin Wang Jabs; Sherri J Bale; John J DiGiovanna; Jouni Uitto; Laura Russell
Journal:  Am J Hum Genet       Date:  2002-03-22       Impact factor: 11.025

5.  Congenital deafness, spiny hyperkeratosis, and universal alopecia.

Authors:  E N Myers; S E Stool; P J Koblenzer
Journal:  Arch Otolaryngol       Date:  1971-01

6.  Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness.

Authors:  Takayuki Kudo; Shigeo Kure; Katsuhisa Ikeda; An-Ping Xia; Yukio Katori; Masaaki Suzuki; Kanako Kojima; Akiko Ichinohe; Yoichi Suzuki; Yoko Aoki; Toshimitsu Kobayashi; Yoichi Matsubara
Journal:  Hum Mol Genet       Date:  2003-05-01       Impact factor: 6.150

7.  Fatal septicemia in an infant with keratitis, ichthyosis, and deafness (KID) syndrome.

Authors:  Amy Gilliam; Mary L Williams
Journal:  Pediatr Dermatol       Date:  2002 May-Jun       Impact factor: 1.588

8.  Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns.

Authors:  Tomohiro Oguchi; Akihiro Ohtsuka; Shigenari Hashimoto; Aki Oshima; Satoko Abe; Yumiko Kobayashi; Kyoko Nagai; Tatsuo Matsunaga; Satoshi Iwasaki; Takashi Nakagawa; Shin-Ichi Usami
Journal:  J Hum Genet       Date:  2005-02-08       Impact factor: 3.172

9.  Deoxyribonucleic acid contamination in archival human temporal bones: a potentially significant problem.

Authors:  Michael J McKenna; Arthur G Kristiansen; Anke S Tropitzsch; Lisbeth Tranebjaerg; Saumil N Merchant
Journal:  Otol Neurotol       Date:  2002-09       Impact factor: 2.311

Review 10.  Human nonsyndromic sensorineural deafness.

Authors:  Thomas B Friedman; Andrew J Griffith
Journal:  Annu Rev Genomics Hum Genet       Date:  2003       Impact factor: 8.929

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  20 in total

Review 1.  Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome.

Authors:  Noah A Levit; Gulistan Mese; Mena-George R Basaly; Thomas W White
Journal:  Biochim Biophys Acta       Date:  2011-09-10

2.  Charge at the 46th residue of connexin 50 is crucial for the gap-junctional unitary conductance and transjunctional voltage-dependent gating.

Authors:  Xiaoling Tong; Hiroshi Aoyama; Tomitake Tsukihara; Donglin Bai
Journal:  J Physiol       Date:  2014-09-25       Impact factor: 5.182

Review 3.  Biological role of connexin intercellular channels and hemichannels.

Authors:  Rekha Kar; Nidhi Batra; Manuel A Riquelme; Jean X Jiang
Journal:  Arch Biochem Biophys       Date:  2012-03-17       Impact factor: 4.013

4.  Temporal bone abnormalities in children with GJB2 mutations.

Authors:  Margaret A Kenna; Heidi L Rehm; Anna Frangulov; Henry A Feldman; Caroline D Robson
Journal:  Laryngoscope       Date:  2011-02-04       Impact factor: 3.325

Review 5.  Connexin channel and its role in diabetic retinopathy.

Authors:  Sayon Roy; Jean X Jiang; An-Fei Li; Dongjoon Kim
Journal:  Prog Retin Eye Res       Date:  2017-06-08       Impact factor: 21.198

Review 6.  Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models.

Authors:  Emilie Hoang Dinh; Shoeb Ahmad; Qing Chang; Wenxue Tang; Benjamin Stong; Xi Lin
Journal:  Brain Res       Date:  2009-02-20       Impact factor: 3.252

7.  Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome.

Authors:  Helmuth A Sánchez; Gülistan Mese; Miduturu Srinivas; Thomas W White; Vytas K Verselis
Journal:  J Gen Physiol       Date:  2010-07       Impact factor: 4.086

8.  Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean population.

Authors:  Sung-Hee Han; Hong-Joon Park; Eun-Joo Kang; Jae-Song Ryu; Anna Lee; Young-Ho Yang; Kyoung-Ryul Lee
Journal:  J Hum Genet       Date:  2008-12-02       Impact factor: 3.172

Review 9.  Cochlear histopathology in human genetic hearing loss: State of the science and future prospects.

Authors:  Krishna Bommakanti; Janani S Iyer; Konstantina M Stankovic
Journal:  Hear Res       Date:  2019-08-19       Impact factor: 3.208

10.  The D50N mutation and syndromic deafness: altered Cx26 hemichannel properties caused by effects on the pore and intersubunit interactions.

Authors:  Helmuth A Sanchez; Krista Villone; Miduturu Srinivas; Vytas K Verselis
Journal:  J Gen Physiol       Date:  2013-07       Impact factor: 4.086

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