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