Autosomal dominant spastic paraplegia type 36
Synonyms: SPG36
A complex form of hereditary spastic paraplegia characterized by an onset in childhood or adulthood of progressive spastic paraplegia (with spastic gait spasticity lower limb weakness pes cavus and urinary urgency) associated with the additional manifestation of peripheral sensorimotor neuropathy.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
Newly diagnosed with
Autosomal dominant spastic paraplegia type 36?
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Advocacy Organizations
KIF1A.ORG
KIF1A.ORG is a global community dedicated to improving the lives of those affected by KIF1A Associated Neurological Disorder (KAND) and accelerating research to find a cure.
National Ataxia Foundation
To accelerate the development of treatments and a cure while working to improve the lives of those living with Ataxia.
Clinical Trials
For a list of clinical trials in this disease area, please click here.