Literature DB >> 14535568

Worldwide distribution of Waardenburg syndrome.

Chetan S Nayak1, Glenn Isaacson.   

Abstract

To clarify the multiracial occurrence of Waardenburg syndrome, we present a case series and literature review. A computerized review of the English-language literature was conducted to assess the distribution of reported occurrences of Waardenburg syndrome in populations around the world. We detail the clinical features of 2 family cohorts: one of Western European origin and the other from South Asia. A computerized literature review found sporadic cases of the syndrome in many ethnic groups, including Japanese, Taiwanese, and Middle Eastern families. The highest reported incidence is among Kenyan Africans. Waardenburg syndrome accounts for between 2% and 5% of cases of congenital deafness. It was first described in Northern European cohorts and is widely identified in fair-skinned populations. We hope to raise awareness of the worldwide distribution of this important cause of hearing loss.

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Year:  2003        PMID: 14535568     DOI: 10.1177/000348940311200913

Source DB:  PubMed          Journal:  Ann Otol Rhinol Laryngol        ISSN: 0003-4894            Impact factor:   1.547


  24 in total

1.  Systematic discovery of nonobvious human disease models through orthologous phenotypes.

Authors:  Kriston L McGary; Tae Joo Park; John O Woods; Hye Ji Cha; John B Wallingford; Edward M Marcotte
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-22       Impact factor: 11.205

2.  Teaching an old dog new tricks: SINEs of canine genomic diversity.

Authors:  Richard Cordaux; Mark A Batzer
Journal:  Proc Natl Acad Sci U S A       Date:  2006-01-23       Impact factor: 11.205

3.  Paediatric Cochlear Implantation in Patients with Waardenburg Syndrome.

Authors:  Josephine W I van Nierop; Rebecca R Snabel; Margreet Langereis; Ronald J E Pennings; Ronald J C Admiraal; Emmanuel A M Mylanus; Henricus P M Kunst
Journal:  Audiol Neurootol       Date:  2016-06-01       Impact factor: 1.854

4.  Waardenburg syndrome: A rare case with bilateral congenital cataract: An unusual entity.

Authors:  Nitin Vichare; N Bhargava
Journal:  Med J Armed Forces India       Date:  2012-12-01

5.  Shah-Waardenburg syndrome: a case highlighting the importance of a holistic approach to assessing a child.

Authors:  Amogh Patil; Lanka Prathyusha; Muganagowda Patil
Journal:  BMJ Case Rep       Date:  2017-12-22

Review 6.  Syndromic Hearing Loss: A Brief Review of Common Presentations and Genetics.

Authors:  John D Gettelfinger; John P Dahl
Journal:  J Pediatr Genet       Date:  2018-01-04

Review 7.  Cochlear implantation in common forms of genetic deafness.

Authors:  Richard J Vivero; Kenneth Fan; Simon Angeli; Thomas J Balkany; Xue Z Liu
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2010-07-22       Impact factor: 1.675

8.  Retrotransposon insertion in SILV is responsible for merle patterning of the domestic dog.

Authors:  Leigh Anne Clark; Jacquelyn M Wahl; Christine A Rees; Keith E Murphy
Journal:  Proc Natl Acad Sci U S A       Date:  2006-01-09       Impact factor: 11.205

9.  A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1.

Authors:  Filiz Hazan; A Taylan Ozturk; Hamit Adibelli; Nurettin Unal; Ajlan Tukun
Journal:  Mol Vis       Date:  2013-01-29       Impact factor: 2.367

10.  High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing.

Authors:  Sen Zhang; Hongen Xu; Yongan Tian; Danhua Liu; Xinyue Hou; Beiping Zeng; Bei Chen; Huanfei Liu; Ruijun Li; Xiaohua Li; Bin Zuo; Ryan Tang; Wenxue Tang
Journal:  Front Genet       Date:  2021-06-04       Impact factor: 4.599

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