Catalog
Autosomal recessive complex hereditary spastic paraplegia
No MMS code
Link to WHO Definition
Autosomal recessive complex hereditary spastic paraplegia – http://id.who.int/icd/entity/275233463
A term used to describe a group of clinically and genetically heterogenous disorders which are inherited in an autosomal recessive (AR) manner. In addition to the neurological features observed in the uncomplicated (pure) forms of AR HSP, affected individuals with complex HSP may in addition exhibit other neurological features such as ataxia, peripheral neuropathy, deafness, cognitive impairment, epilepsy, ocular involvement, amyotrophy and extrapyramidal involvement.
Parents
Children
- Autosomal recessive spastic paraplegia type 26
- Autosomal recessive spastic paraplegia type 20
- Autosomal recessive spastic paraplegia type 39
- Autosomal recessive spastic paraplegia type 14
- Autosomal recessive spastic paraplegia type 23
- Autosomal recessive spastic paraplegia type 21
- Autosomal recessive spastic paraplegia type 15
- Autosomal recessive spastic paraplegia type 25
- Autosomal recessive spastic paraplegia type 11
- Autosomal recessive spastic paraplegia type 27
- Autosomal recessive spastic paraplegia type 32
- Autosomal recessive spastic paraplegia type 18
- Autosomal recessive complex hereditary spastic paraplegia due to mutations in Spatacsin gene
- Autosomal recessive spastic paraplegia type 35