Portal de Periódicos da CAPES

Artigo Produção Nacional Revisado por pares

BIBTEX RIS

Huntington disease and Huntington disease‐like in a case series from Brazil

2013; Wiley; Volume: 86; Issue: 4 Linguagem: Inglês

10.1111/cge.12283

1399-0004

Raphael Machado Castilhos, Aline Fernanda de Souza, Gabriel Vasata Furtado, Tailise Conte Gheno, André Luíz Reis da Silva, Fernando Regla Vargas, Maria-Angelica Lima, Orlando Graziani Póvoas Barsottini, José Luiz Pedroso, Clécio Godeiro‐Júnior, Diego Zanotti Salarini, Eanes Torres Pereira, Kátia Lin, Maria Betânia Pereira Toralles, Jonas Alex Morales Saute, Carlos Roberto de Mello Rieder, Marlene Quintas, Jorge Sequeiros, Isabel Alonso, Maria Luiza Saraiva Pereira, Laura Bannach Jardim,

Hereditary Neurological Disorders

The aim of this study was to identify the relative frequency of Huntington's disease ( HD ) and HD ‐like (HDL) disorders HDL1 , HDL2 , spinocerebellar ataxia type 2 ( SCA2 ), SCA17 , dentatorubral‐pallidoluysian degeneration ( DRPLA ), benign hereditary chorea, neuroferritinopathy and chorea‐acanthocytosis (CHAC), in a series of Brazilian families. Patients were recruited in seven centers if they or their relatives presented at least chorea, besides other findings. Molecular studies of HTT , ATXN2 , TBP , ATN1 , JPH3 , FTL , NKX2 ‐1/ TITF1 and VPS13A genes were performed. A total of 104 families were ascertained from 2001 to 2012: 71 families from South, 25 from Southeast and 8 from Northeast Brazil. There were 93 HD , 4 HDL2 and 1 SCA2 families. Eleven of 104 index cases did not have a family history: 10 with HD . Clinical characteristics were similar between HD and non‐ HD cases. In HD , the median expanded ( CAG )n (range) was 44 (40–81) units; R 2 between expanded HTT and age‐at‐onset ( AO ) was 0.55 (p = 0.0001, Pearson). HDL2 was found in Rio de Janeiro (2 of 9 families) and Rio Grande do Sul states (2 of 68 families). We detected HD in 89.4%, HDL2 in 3.8% and SCA2 in 1% of 104 Brazilian families. There were no cases of HDL1 , SCA17 , DRPLA , neuroferritinopathy, benign hereditary chorea or CHAC. Only six families (5.8%) remained without diagnosis.