Autosomal dominant hereditary spastic paraplegia
Complicated hereditary spastic paraplegia
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Autosomal dominant spastic paraplegia type 38 (disorder)
Autosomal dominant spastic paraplegia type 38
A complex hereditary spastic paraplegia with characteristics of mild to severe lower limbs spasticity, hyperreflexia, extensor plantar responses, pes cavus and significant wasting and weakness of the small hand muscles. Impaired vibration sensation, temporal lobe epilepsy and cognitive dysfunction were also reported.
autosomaal dominante spastische paraplegie type 38
SPG38
autosomaal dominante spastische paraparese type 38
Id783622001
StatusPrimitive
Associated morphologyDegenerative abnormality
Finding siteSpinal cord structure
Finding siteLower limb structure
Clinical courseProgressive
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetG11.4
RuleTRUE
AdviceALWAYS G11.4
CorrelationSNOMED CT source code to target map code correlation not specified