A Case of Hereditary Spastic Ataxia
Journal of the Korean Neurological Association
;
: 396-400, 1995.
Artículo
en Coreano
| WPRIM
| ID: wpr-7343
ABSTRACT
Hereditary spastic ataxia is a familial neurological disorder which exhibit the features of a progressive combined pyramidal tract and cerebellar deficiency. The main features are progressive gait disturbance, incoordination, nystagmus, visual impairment, hyperreflexia, extensor plantar response, peripheral neuropathy, and pes cavus. A 27-year-old male patient with spastic ataxic gait was evaluated. He showed characteristic features of hereditary spastic ataxia. There were another twelve affected members in four generations of his family which may be inherited by autosomal dominant pattern. One of them is reported with review of the literature on familial spastic ataxia.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Tractos Piramidales
/
Ataxia
/
Trastornos de la Visión
/
Deformidades del Pie
/
Reflejo Anormal
/
Composición Familiar
/
Reflejo de Babinski
/
Enfermedades del Sistema Nervioso Periférico
/
Marcha
/
Espasticidad Muscular
Límite:
Adulto
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Neurological Association
Año:
1995
Tipo del documento:
Artículo
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