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Eur J Neurol ; 23(6): 1134-6, 2016 06.
Artigo em Inglês | MEDLINE | ID: mdl-27141859

RESUMO

BACKGROUND AND PURPOSE: Disease severity varies considerably among patients with Spinal and Bulbar Muscular Atrophy (SBMA). Our aim was to investigate the role of androgen receptor (AR) polymorphic repeats in SBMA phenotype. METHODS: We analyzed the length of AR polyQ and polyG tracts in 159 SBMA patients. RESULTS: No relationship between polyG size or polyG/polyQ haplotypes and clinical phenotype was found. An independent negative correlation between polyQ-length and onset of weakness was confirmed (P < 0.001). CONCLUSIONS: The negative results of our study prompt to continue the search for potential disease modifiers in SBMA outside the AR gene.


Assuntos
Atrofia Muscular Espinal/genética , Polimorfismo de Nucleotídeo Único , Receptores Androgênicos/genética , Alelos , Haplótipos , Humanos , Peptídeos/genética , Fenótipo , Poli G/genética
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