Autosomal Dominant Spastic Paraplegia Type 36
Autosomal dominant spastic paraplegia type 36 (SPG36) is 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.
Genes related to Autosomal Dominant Spastic Paraplegia Type 36
Clinical FeaturesTop most frequent phenotypes and symptoms related to Autosomal Dominant Spastic Paraplegia Type 36
- Peripheral neuropathy
- Babinski sign
- Pes cavus
- Proximal muscle weakness
- Distal muscle weakness
And another 18 symptoms. If you need more information about this disease we can help you.
Incidence and onset information— Based on the latest data available there are 1 families with AUTOSOMAL DOMINANT SPASTIC PARAPLEGIA TYPE 36 in Europe.
— No data available about the known clinical features onset.
Autosomal Dominant Spastic Paraplegia Type 36 Is also known as spg36.
Researches and researchersCurrently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.
Sources and references
You can check the following sources for additional information.ORPHANET OMIM MESH Genetic Syndrome Finder
If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1; VCRL1