A Case of Hereditary Spastic Ataxia
Journal of the Korean Neurological Association
;
: 396-400, 1995.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pyramidal Tracts
/
Ataxia
/
Vision Disorders
/
Foot Deformities
/
Reflex, Abnormal
/
Family Characteristics
/
Reflex, Babinski
/
Peripheral Nervous System Diseases
/
Gait
/
Muscle Spasticity
Limits:
Adult
/
Humans
/
Male
Language:
Korean
Journal:
Journal of the Korean Neurological Association
Year:
1995
Type:
Article
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