Autosomal dominant complex hereditary spastic paraplegia (Q84971): Difference between revisions

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Latest revision as of 10:19, 15 August 2026

A term used to describe a group of clinically and genetically heterogenous disorders which are inherited in an autosomal dominant (AD) manner. In addition to the neurological features observed in the “pure” forms of autosomal dominant HSP, affected individuals with complex (complicated) HSP may in addition exhibit other neurological features such as ataxia, peripheral neuropathy, deafness, cognitive impairment, epilepsy, amyotrophy and extrapyramidal involvement.

Language	Label	Description	Also known as
default for all languages	ID_873077851
English	Autosomal dominant complex hereditary spastic paraplegia	A term used to describe a group of clinically and genetically heterogenous disorders which are inherited in an autosomal dominant (AD) manner. In addition to the neurological features observed in the “pure” forms of autosomal dominant HSP, affected individuals with complex (complicated) HSP may in addition exhibit other neurological features such as ataxia, peripheral neuropathy, deafness, cognitive impairment, epilepsy, amyotrophy and extrapyramidal involvement.