Autosomal dominant spastic paraplegia type 73

Orpha code: 444099OMIM code: 616282

Definition

A pure form of hereditary spastic paraplegia characterized by adult onset of crural spastic paraparesis, hyperreflexia, extensor plantar responses, proximal muscle weakness, mild muscle atrophy, decreased vibration sensation at ankles, and mild urinary dysfunction. Foot deformities have been reported to eventually occur in some patients. No abnormalities are noted on brain magnetic resonance imaging and peripheral nerve conduction velocity studies.

Disease data
Classification

Disease

Synonyms
SPG73
SPG73
ORPHA code
444099
OMIM code
616282
ICD10 code
G11.4
ICD11 code
-

No additional description.

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