Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imaging.
Mov Disord
; 10(4): 513-7, 1995 Jul.
Article
em En
| MEDLINE
| ID: mdl-7565837
ABSTRACT
We report two families with a disorder, probably autosomal recessive, characterized by tremor of juvenile onset, dystonia, and myoclonus with preserved cognitive, cerebellar, and peripheral nervous system functions. During 4 years' follow-up, mild spasticity appeared. Magnetic resonance imaging (MRI) revealed mild diffuse changes in the white matter. Central conduction times for visual, motor, and sensory systems were all prolonged. Extensive metabolic work-up failed to reveal lysosomal, peroxisomal, mitochondrial, or other metabolic abnormalities.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Tremor
/
Encefalopatias Metabólicas
/
Imageamento por Ressonância Magnética
/
Distonia
/
Mioclonia
Tipo de estudo:
Diagnostic_studies
/
Observational_studies
/
Prognostic_studies
Limite:
Adolescent
/
Adult
/
Child
/
Female
/
Humans
/
Male
País/Região como assunto:
Asia
Idioma:
En
Revista:
Mov Disord
Assunto da revista:
NEUROLOGIA
Ano de publicação:
1995
Tipo de documento:
Article
País de afiliação:
Arábia Saudita