Literature DB >> 15178965

Epidemiology of Usher syndrome in Valencia and Spain.

C Espinós1, J M Millán, M Beneyto, C Nájera.   

Abstract

OBJECTIVE: To obtain epidemiological data on the prevalence of the different types of Usher syndrome (US) in Spain, since these data were missing; to estimate the proportion of sporadic cases among simplex families, and calculate the prevalence of the Usher syndrome in a homogeneous population from Eastern Spain (3,875,234 inhabitants) that is representative of the Spanish population.
METHODS: Otological, ophthalmological and genetic studies were performed in 89 US patients from 46 families and subjected to statistical and segregation analysis.
RESULTS: 41.6% of them suffered US type I, 46.1% type II, and in 12.3% the classification remains unclear. The estimated prevalence for the Province of Valencia was 4.2/100,000. There was a notable excess of male-only affected multiplex sibships in our sample that could be attributable to an X-linked inheritance.
CONCLUSIONS: The number of families with USI type was similar to that of families with USII type. The estimated prevalence for the Province of Valencia is in agreement with other reports in which the estimate for the prevalence of US ranges from 1.8 to 6.2/100,000.

Entities:  

Year:  1998        PMID: 15178965     DOI: 10.1159/000016167

Source DB:  PubMed          Journal:  Community Genet        ISSN: 1422-2795


  21 in total

Review 1.  Genetics and pathological mechanisms of Usher syndrome.

Authors:  Denise Yan; Xue Z Liu
Journal:  J Hum Genet       Date:  2010-04-09       Impact factor: 3.172

2.  Mutational screening of the USH2A gene in Spanish USH patients reveals 23 novel pathogenic mutations.

Authors:  Gema Garcia-Garcia; Maria J Aparisi; Teresa Jaijo; Regina Rodrigo; Ana M Leon; Almudena Avila-Fernandez; Fiona Blanco-Kelly; Sara Bernal; Rafael Navarro; Manuel Diaz-Llopis; Montserrat Baiget; Carmen Ayuso; Jose M Millan; Elena Aller
Journal:  Orphanet J Rare Dis       Date:  2011-10-17       Impact factor: 4.123

3.  Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II.

Authors:  E Aller; T Jaijo; M Beneyto; C Nájera; S Oltra; C Ayuso; M Baiget; M Carballo; G Antiñolo; D Valverde; F Moreno; C Vilela; D Collado; H Pérez-Garrigues; A Navea; J M Millán
Journal:  J Med Genet       Date:  2006-11       Impact factor: 6.318

4.  Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing loss.

Authors:  Heather A Stiff; Christina M Sloan-Heggen; Ashley Ko; Wanda L Pfeifer; Diana L Kolbe; Carla J Nishimura; Kathy L Frees; Kevin T Booth; Donghong Wang; Amy E Weaver; Hela Azaiez; John Kamholz; Richard J H Smith; Arlene V Drack
Journal:  Ophthalmic Genet       Date:  2020-04-13       Impact factor: 1.803

5.  CEP78 is mutated in a distinct type of Usher syndrome.

Authors:  Qing Fu; Mingchu Xu; Xue Chen; Xunlun Sheng; Zhisheng Yuan; Yani Liu; Huajin Li; Zixi Sun; Huiping Li; Lizhu Yang; Keqing Wang; Fangxia Zhang; Yumei Li; Chen Zhao; Ruifang Sui; Rui Chen
Journal:  J Med Genet       Date:  2016-09-14       Impact factor: 6.318

6.  Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I.

Authors:  A Oshima; T Jaijo; E Aller; J M Millan; C Carney; S Usami; C Moller; W J Kimberling
Journal:  Hum Mutat       Date:  2008-06       Impact factor: 4.878

7.  Novel mutations in the USH1C gene in Usher syndrome patients.

Authors:  María José Aparisi; Gema García-García; Teresa Jaijo; Regina Rodrigo; Claudio Graziano; Marco Seri; Tulay Simsek; Enver Simsek; Sara Bernal; Montserrat Baiget; Herminio Pérez-Garrigues; Elena Aller; José María Millán
Journal:  Mol Vis       Date:  2010-12-31       Impact factor: 2.367

8.  An update on the genetics of usher syndrome.

Authors:  José M Millán; Elena Aller; Teresa Jaijo; Fiona Blanco-Kelly; Ascensión Gimenez-Pardo; Carmen Ayuso
Journal:  J Ophthalmol       Date:  2010-12-23       Impact factor: 1.909

9.  Study of USH1 splicing variants through minigenes and transcript analysis from nasal epithelial cells.

Authors:  María José Aparisi; Gema García-García; Elena Aller; María Dolores Sequedo; Cristina Martínez-Fernández de la Cámara; Regina Rodrigo; Miguel Armengot; Julio Cortijo; Javier Milara; Manuel Díaz-LLopis; Teresa Jaijo; José María Millán
Journal:  PLoS One       Date:  2013-02-25       Impact factor: 3.240

10.  Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures.

Authors:  Danilo Licastro; Margherita Mutarelli; Ivana Peluso; Kornelia Neveling; Nienke Wieskamp; Rossella Rispoli; Diego Vozzi; Emmanouil Athanasakis; Angela D'Eustacchio; Mariateresa Pizzo; Francesca D'Amico; Carmela Ziviello; Francesca Simonelli; Antonella Fabretto; Hans Scheffer; Paolo Gasparini; Sandro Banfi; Vincenzo Nigro
Journal:  PLoS One       Date:  2012-08-29       Impact factor: 3.240

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