Please use this identifier to cite or link to this item:
Type: Artigo de periódico
Title: Leber's hereditary optic neuropathy: Clinical and molecular profile of a Brazilian sample
Author: Maciel-Guerra, AT
Zanchetta, LM
Fernandes, MSA
Andrade, PB
Miranda, PMDD
Sartorato, EL
Abstract: Purpose: The aim of this study was to describe clinical features and search for primary mitochondrial DNA (mtDNA) mutations in 13 unrelated Brazilian patients with Leber's hereditary optic neuropathy (LHON). Methods: Analysis of the G11778A, G3460A, and T14484C mutations was done by polymerase chain reaction and restriction fragment length polymorphism, and mutations were confirmed by direct sequencing. Mean age of onset was 24.5 years and all cases were bilateral. Results: Sex ratio (12M:1F) and frequency of simultaneous involvement (9/13) were higher than in other studies. In nine cases there was familial recurrence: 24 male and two female relatives. Ten patients had a mutation: G11778A in six, T14484C in three and one G3460A. The frequency of patients bearing a primary mutation was lower than that described in multicentric studies but similar to that observed among Asians. A higher frequency of the T14484C mutation was detected. Conclusions: The contribution of Amerindians and Africans to the Brazilian mtDNA pool may account for differences in the type and frequency of primary LHON mutations.
Subject: optic nerve diseases
Leber's hereditary optic neuropathy
Country: EUA
Editor: Taylor & Francis Inc
Rights: fechado
Identifier DOI: 10.3109/13816810.2010.483721
Date Issue: 2010
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
WOS000282248100004.pdf506.8 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.