Catalog
Autosomal dominant complex hereditary spastic paraplegia
No MMS code
Link to WHO Definition
Autosomal dominant complex hereditary spastic paraplegia – http://id.who.int/icd/entity/873077851
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.
Parents
Children
- Autosomal dominant spastic paraplegia type 29
- Autosomal dominant spastic paraplegia type 38
- Autosomal dominant spastic paraplegia type 37
- Autosomal dominant spastic paraplegia type 9
- Autosomal dominant spastic paraplegia type 17
- Autosomal dominant complex hereditary spastic paraplegia due to mutations in Spastin gene