Hereditary spastic paraplegia
Hereditary spastic paraplegia (HSP) was first reported by Seeligmuller (1874). It is a syndrome characterized by progressive hypertonia, weakness and scissor gait in the lower limbs. The clinical manifestations are mainly slow-progressing spastic paraplegia with various symptoms. Most scholars classify it as hereditary ataxia, accounting for about 1/4 of the total incidence of the latter.
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Site of disease:
spinal cord -
Infectious :
Not contagious -
Frequent population:
Most often present in childhood or adolescence -
Related symptoms:
Ataxia Visual impairment Hyperflexia Hypertonia Spastic paraplegic gait -
Concurrent disease:
Related Drugs
Baclofen
Indication: No data yet
Manufacturer:
Fuan Pharmaceutical Group Ningbo Team Pharmaceutical Co., Ltd.
Related Ingredients