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Huntington disease: DNA analysis in brazilian population

Authors :
RASKIN SALMO
ALLAN NASSER
TEIVE HÉLIO A.G.
CARDOSO FRANCISCO
HADDAD MÔNICA SANTORO
LEVI GILBERTO
BOY RAQUEL
LERENA JR JUAN
SOTOMAIOR VANESSA SANTOS
JANZEN-DÜCK MÔNICA
JARDIM LAURA BANNACH
FELLANDER FLÁVIO R.
ANDRADE LUIZ AUGUSTO FRANCO
Source :
Arquivos de Neuro-Psiquiatria, Vol 58, Iss 4, Pp 977-985 (2000)
Publication Year :
2000
Publisher :
Academia Brasileira de Neurologia (ABNEURO), 2000.

Abstract

Huntington disease (HD) is associated with expansions of a CAG trinucleotide repeat in the HD gene. Accurate measurement of a specific CAG repeat sequence in the HD gene in 92 Brazilian controls without HD, 44 Brazilian subjects with clinical findings suggestive of HD and 40 individuals from 6 putative HD families, showed a range from 7 to 33 repeats in normal subjects and 39 to 88 repeats in affected subjects. A trend between early age at onset of first symptoms and increasing number of repeats was seen. Major increase of repeat size through paternal inheritance than through maternal inheritance was observed. Data generated from this study may have significant implications for the etiology, knowledge of the incidence, diagnosis, prognosis, genetic counseling and treatment of HD Brazilian patients.

Details

Language :
English
ISSN :
0004282X and 16784227
Volume :
58
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Arquivos de Neuro-Psiquiatria
Publication Type :
Academic Journal
Accession number :
edsdoj.2e4001b00f3d41ed9413934f8c90b0e7
Document Type :
article