Literature DB >> 12752120

Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome.

S Yotsumoto1, T Hashiguchi, X Chen, N Ohtake, A Tomitaka, H Akamatsu, K Matsunaga, S Shiraishi, H Miura, J Adachi, T Kanzaki.   

Abstract

BACKGROUND: Germline missense mutations in the GJB2 gene that encodes connexin-26 (Cx26) have recently been found to be the cause of the keratitis-ichthyosis-deafness (KID) syndrome.
OBJECTIVES: To define the GJB2 mutations in three Japanese patients with KID syndrome.
METHODS: Genomic DNA was extracted from peripheral blood and used to amplify the GJB2 gene. Direct sequencing and endonuclease digestion were used for mutation analysis and DNA-based diagnosis.
RESULTS: We identified two heterozygous mis-sense mutations (D50Y, D50N) in the GJB2 gene in three Japanese patients with KID syndrome. All mutations were located on the first extracellular domain of Cx26.
CONCLUSIONS: These data expand the GJB2 mutation database and show that a dominant mutation of Cx26 can cause KID syndrome in Japanese patients.

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Year:  2003        PMID: 12752120     DOI: 10.1046/j.1365-2133.2003.05245.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  18 in total

1.  A novel N14Y mutation in Connexin26 in keratitis-ichthyosis-deafness syndrome: analyses of altered gap junctional communication and molecular structure of N terminus of mutated Connexin26.

Authors:  Ken Arita; Masashi Akiyama; Tomoyasu Aizawa; Yoshitaka Umetsu; Ikuo Segawa; Maki Goto; Daisuke Sawamura; Makoto Demura; Keiichi Kawano; Hiroshi Shimizu
Journal:  Am J Pathol       Date:  2006-08       Impact factor: 4.307

Review 2.  Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.

Authors:  Niloofar Bazazzadegan; Abraham M Sheffield; Masoomeh Sobhani; Kimia Kahrizi; Nicole C Meyer; Guy Van Camp; Nele Hilgert; Seyedeh Sedigheh Abedini; Farkhondeh Habibi; Ahmad Daneshi; Carla Nishimura; Matthew R Avenarius; Mohammad Farhadi; Richard J H Smith; Hossein Najmabadi
Journal:  Am J Med Genet A       Date:  2011-04-11       Impact factor: 2.802

3.  A Novel GJB2 compound heterozygous mutation c.257C>G (p.T86R)/c.176del16 (p.G59A fs*18) causes sensorineural hearing loss in a Chinese family.

Authors:  Xi Shi; Yan Zhang; Shiwei Qiu; Wei Zhuang; Na Yuan; Tiantian Sun; Jian Gao; Yuehua Qiao; Ke Liu
Journal:  J Clin Lab Anal       Date:  2018-04-17       Impact factor: 2.352

Review 4.  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

5.  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

6.  Some oculodentodigital dysplasia-associated Cx43 mutations cause increased hemichannel activity in addition to deficient gap junction channels.

Authors:  Radoslaw Dobrowolski; Annette Sommershof; Klaus Willecke
Journal:  J Membr Biol       Date:  2007-08-09       Impact factor: 1.843

Review 7.  Autosomal recessive nonsyndromic deafness genes: a review.

Authors:  Duygu Duman; Mustafa Tekin
Journal:  Front Biosci (Landmark Ed)       Date:  2012-06-01

8.  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

9.  GJB2 Gene Mutations in Syndromic Skin Diseases with Sensorineural Hearing Loss.

Authors:  Sandra Iossa; Elio Marciano; Annamaria Franzé
Journal:  Curr Genomics       Date:  2011-11       Impact factor: 2.236

10.  Phenotypic variability in gap junction syndromic skin disorders: experience from KID and Clouston syndromes' clinical diagnostics.

Authors:  Anna Kutkowska-Kaźmierczak; Katarzyna Niepokój; Katarzyna Wertheim-Tysarowska; Aleksandra Giza; Maria Mordasewicz-Goliszewska; Jerzy Bal; Ewa Obersztyn
Journal:  J Appl Genet       Date:  2015-01-10       Impact factor: 3.240

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