Literature DB >> 17666888

A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort.

Girish V Putcha1, Bassem A Bejjani, Stacey Bleoo, Jessica K Booker, John C Carey, Nancy Carson, Soma Das, Melissa A Dempsey, Julie M Gastier-Foster, John H Greinwald, Marcy L Hoffmann, Linda Jo Bone Jeng, Margaret A Kenna, Ishrag Khababa, Margaret Lilley, Rong Mao, Kasinathan Muralidharan, Iris M Otani, Heidi L Rehm, Fred Schaefer, William K Seltzer, Elaine B Spector, Michelle A Springer, Karen E Weck, Richard J Wenstrup, Stacey Withrow, Bai-Lin Wu, Maimoona A Zariwala, Iris Schrijver.   

Abstract

PURPOSE: The aim of the study was to determine the actual GJB2 and GJB6 mutation frequencies in North America after several years of generalized testing for autosomal recessive nonsyndromic sensorineural hearing loss to help guide diagnostic testing algorithms, especially in light of molecular diagnostic follow-up to universal newborn hearing screening.
METHODS: Mutation types, frequencies, ethnic distributions, and genotype-phenotype correlations for GJB2 and GJB6 were assessed in a very large North American cohort.
RESULTS: GJB2 variants were identified in 1796 (24.3%) of the 7401 individuals examined, with 399 (5.4%) homozygous and 429 (5.8%) compound heterozygous. GJB6 deletion testing was performed in 12.0% (888/7401) of all cases. The >300-kb deletion was identified in only nine individuals (1.0%), all of whom were compound heterozygous for mutations in GJB2 and GJB6. Among a total of 139 GJB2 variants identified, 53 (38.1%) were previously unreported, presumably representing novel pathogenic or benign variants.
CONCLUSIONS: The frequency and distribution of sequence changes in GJB2 and GJB6 in North America differ from those previously reported, suggesting a considerable role for loci other than GJB2 and GJB6 in the etiology of autosomal recessive nonsyndromic sensorineural hearing loss, with minimal prevalence of the GJB6 deletion.

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Year:  2007        PMID: 17666888     DOI: 10.1097GIM.0b013e3180a03276

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  32 in total

1.  Infrequency of two deletion mutations at the DFNB1 locus in patients and controls.

Authors:  Hsiao-Yuan Tang; Monica J Basehore; Gregory L Blakey; Sandra Darilek; John S Oghalai; Benjamin B Roa; Ping Fang; Raye Lynn Alford
Journal:  Am J Med Genet A       Date:  2008-04-01       Impact factor: 2.802

Review 2.  The Genetic Basis of Nonsyndromic Hearing Loss in Indian and Pakistani Populations.

Authors:  Denise Yan; Abhiraami Kannan-Sundhari; Subramanian Vishwanath; Jie Qing; Rahul Mittal; Mohan Kameswaran; Xue Zhong Liu
Journal:  Genet Test Mol Biomarkers       Date:  2015-07-17

3.  Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.

Authors:  Qianqian Zhu; Dongliang Ge; Erin L Heinzen; Samuel P Dickson; Thomas J Urban; Mingfu Zhu; Jessica M Maia; Min He; Qian Zhao; Kevin V Shianna; David B Goldstein
Journal:  Am J Hum Genet       Date:  2012-08-30       Impact factor: 11.025

4.  Comprehensive diagnostic battery for evaluating sensorineural hearing loss in children.

Authors:  Jerry W Lin; Naweed Chowdhury; Avni Mody; Ross Tonini; Claudia Emery; Jody Haymond; John S Oghalai
Journal:  Otol Neurotol       Date:  2011-02       Impact factor: 2.311

5.  Functional evaluation of GJB2 variants in nonsyndromic hearing loss.

Authors:  Soo-Young Choi; Kyu Yup Lee; Hyun-Jin Kim; Hyo-Kyeong Kim; Qing Chang; Hong-Joon Park; Chang-Jin Jeon; Xi Lin; Jinwoong Bok; Un-Kyung Kim
Journal:  Mol Med       Date:  2011-01-08       Impact factor: 6.354

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.  High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays.

Authors:  Prachi Kothiyal; Stephanie Cox; Jonathan Ebert; Ammar Husami; Margaret A Kenna; John H Greinwald; Bruce J Aronow; Heidi L Rehm
Journal:  BMC Biotechnol       Date:  2010-02-10       Impact factor: 2.563

9.  Genotyping with a 198 mutation arrayed primer extension array for hereditary hearing loss: assessment of its diagnostic value for medical practice.

Authors:  Juan Rodriguez-Paris; Lynn Pique; Tahl Colen; Joseph Roberson; Phyllis Gardner; Iris Schrijver
Journal:  PLoS One       Date:  2010-07-26       Impact factor: 3.240

10.  Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss.

Authors:  Christopher Beck; Jose Carmelo Pérez-Álvarez; Alexander Sigruener; Frank Haubner; Till Seidler; Charalampos Aslanidis; Jürgen Strutz; Gerd Schmitz
Journal:  Eur Arch Otorhinolaryngol       Date:  2014-09-12       Impact factor: 2.503

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