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Up to: Autosomal dominant complex spastic paraplegia
Spastic paraplegia-facial-cutaneous lesions syndrome
Spastic paraplegia-facial-cutaneous lesions syndrome is a complex form of hereditary spastic paraplegia characterized by delays in motor development followed by a slowly progressive spastic paraplegia (affecting mainly lower extremities) associated with a desquamating facial rash with butterfly distribution (presenting at around two months of age) and dysarthria. There have been no further descriptions in the literature since 1982.
This condition has no sub-types.