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[Mutational frequencies in usherin(USH2A gene) in 26 Colombian individuals with Usher syndrome type II]. / Frecuencia de mutaciones en el gen de la usherina (USH2A) en 26 individuos colombianos con síndrome de Usher, tipo II.
López, Greizy; Gelvez, Nancy Yaneth; Tamayo, Martalucía.
Afiliação
  • López G; Instituto de Genética Humana, Pontificia Universidad Javeriana, Bogotá, D.C, Colombia.
Biomedica ; 31(1): 82-90, 2011 Mar.
Article em Es | MEDLINE | ID: mdl-22159486
INTRODUCTION: Usher syndrome is a disorder characterized by progressive retinitis pigmentosa, prelingual sensory hearing loss and vestibular dysfunction. It is the most frequent cause of deaf-blindness in humans. Three clinical types and twelve genetic subtypes have been characterized. Type II is the most common, and among these cases, nearly 80% have mutations in the USH2A gene. OBJECTIVE: The aim of the study was to establish the mutational frequencies for the short isoform of USH2A gene in Usher syndrome type II. MATERIALS AND METHODS: Twenty-six Colombian individuals with Usher syndrome type II were included. SSCP analysis for 20 exons of the short isoform was performed and abnormal patterns were sequenced. Sequencing of exon 13 of the USH2A gene was performed for all the individuals because the most frequent mutation is located in this exon. RESULTS: The most frequent mutation was c.2299delG, identified in the 27% (n=8) of the sample. The second mutation, p.R334W, showed a frequency of 15%. A new variant identified in the 5'UTR region, g.129G>T, was present in 1 individual (4%). Four polymorphisms were identified; one of them is a new deletion in exon 20, first reported in this study. CONCLUSIONS: Mutations in the usherin short isoform were identified in 38% of a sample of 26 USH2 cases. Molecular diagnosis was established in 7 of the 26.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas da Matriz Extracelular / Síndromes de Usher / Taxa de Mutação / Mutação Limite: Female / Humans / Male País/Região como assunto: America do sul / Colombia Idioma: Es Revista: Biomedica Ano de publicação: 2011 Tipo de documento: Article País de afiliação: Colômbia País de publicação: Colômbia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas da Matriz Extracelular / Síndromes de Usher / Taxa de Mutação / Mutação Limite: Female / Humans / Male País/Região como assunto: America do sul / Colombia Idioma: Es Revista: Biomedica Ano de publicação: 2011 Tipo de documento: Article País de afiliação: Colômbia País de publicação: Colômbia