Literature DB >> 34387732

First glance at the molecular etiology of hearing loss in French-Canadian families from Saguenay-Lac-Saint-Jean's founder population.

Tania Cruz Marino1, Jessica Tardif2, Josianne Leblanc2, Janie Lavoie3, Pascal Morin3, Michel Harvey3, Marie-Jacqueline Thomas2, Annabelle Pratte2, Nancy Braverman4.   

Abstract

The French-Canadian population of Saguenay-Lac-Saint-Jean is known for its homogenous genetic background. The hereditary causes of hearing loss were previously unexplored in this population. Individuals with hearing loss were referred from the otorhinolaryngology, pediatrics and family physicians' clinics to the medical genetics service at the Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-Saint-Jean between June 2015 and March 2021. A regional clinical evaluation strategy was developed. Samples from 63 individuals belonging to 41 families were sent independently to different molecular clinical laboratories and index cases were analyzed through comprehensive multigene panels, with a diagnostic rate of 54%. Sixteen hearing loss causal variants were identified in 12 genes, with eight of these variants not been previously reported in the literature. Recurrent variants were present in four genes, suggesting a possible founder effect, while GJB2 gene variants were scarce. A comprehensive multigene panel approach as part of the proposed clinical evaluation strategy offers a high diagnostic yield for this population.
© 2021. Crown.

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Year:  2021        PMID: 34387732     DOI: 10.1007/s00439-021-02332-w

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  57 in total

1.  Identification of a novel missense mutation in the WFS1 gene as a cause of autosomal dominant nonsyndromic sensorineural hearing loss in all-frequencies.

Authors:  Xiaohui Bai; Huaiqing Lv; Fengguo Zhang; Jinzhi Liu; Zhaomin Fan; Lei Xu; Yuhang Han; Renjie Chai; Jianfeng Li; Haibo Wang
Journal:  Am J Med Genet A       Date:  2014-09-23       Impact factor: 2.802

2.  Uses and abuses of hearing loss classification.

Authors:  J G Clark
Journal:  ASHA       Date:  1981-07

3.  A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effect.

Authors:  Nelly Abdelfatah; Nancy Merner; Jim Houston; Tammy Benteau; Anne Griffin; Lance Doucette; Tracy Stockley; Julie L Lauzon; Terry-Lynn Young
Journal:  Hum Mutat       Date:  2012-10-11       Impact factor: 4.878

4.  Genetic epidemiology of autosomal recessive spastic ataxia of Charlevoix-Saguenay in northeastern Quebec.

Authors:  M De Braekeleer; F Giasson; J Mathieu; M Roy; J P Bouchard; K Morgan
Journal:  Genet Epidemiol       Date:  1993       Impact factor: 2.135

5.  Genetic epidemiology of sensorimotor polyneuropathy with or without agenesis of the corpus callosum in northeastern Quebec.

Authors:  M De Braekeleer; A Dallaire; J Mathieu
Journal:  Hum Genet       Date:  1993-04       Impact factor: 4.132

6.  PDZD7 and hearing loss: More than just a modifier.

Authors:  Kevin T Booth; Hela Azaiez; Kimia Kahrizi; Allen C Simpson; William T A Tollefson; Christina M Sloan; Nicole C Meyer; Mojgan Babanejad; Fariba Ardalani; Sanaz Arzhangi; Michael J Schnieders; Hossein Najmabadi; Richard J H Smith
Journal:  Am J Med Genet A       Date:  2015-09-29       Impact factor: 2.802

7.  Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-Jean.

Authors:  M De Braekeleer; J Larochelle
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

8.  American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss.

Authors:  Raye L Alford; Kathleen S Arnos; Michelle Fox; Jerry W Lin; Christina G Palmer; Arti Pandya; Heidi L Rehm; Nathaniel H Robin; Daryl A Scott; Christine Yoshinaga-Itano
Journal:  Genet Med       Date:  2014-03-20       Impact factor: 8.822

9.  Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.

Authors:  Guney Bademci; Joseph Foster; Nejat Mahdieh; Mortaza Bonyadi; Duygu Duman; F Basak Cengiz; Ibis Menendez; Oscar Diaz-Horta; Atefeh Shirkavand; Sirous Zeinali; Asli Subasioglu; Suna Tokgoz-Yilmaz; Fabiola Huesca-Hernandez; Maria de la Luz Arenas-Sordo; Juan Dominguez-Aburto; Edgar Hernandez-Zamora; Paola Montenegro; Rosario Paredes; Germania Moreta; Rodrigo Vinueza; Franklin Villegas; Santiago Mendoza-Benitez; Shengru Guo; Nazim Bozan; Tulay Tos; Armagan Incesulu; Gonca Sennaroglu; Susan H Blanton; Hatice Ozturkmen-Akay; Muzeyyen Yildirim-Baylan; Mustafa Tekin
Journal:  Genet Med       Date:  2015-07-30       Impact factor: 8.822

10.  Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients.

Authors:  D Baux; C Vaché; C Blanchet; M Willems; C Baudoin; M Moclyn; V Faugère; R Touraine; B Isidor; D Dupin-Deguine; M Nizon; M Vincent; S Mercier; C Calais; G García-García; Z Azher; L Lambert; Y Perdomo-Trujillo; F Giuliano; M Claustres; M Koenig; M Mondain; A F Roux
Journal:  Sci Rep       Date:  2017-12-01       Impact factor: 4.379

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