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Autosomal dominant spastic paraplegia type 36
Disease definition
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.
ORPHA:320365
Classification level: Disorder- Synonym(s):
- SPG36
- Prevalence: <1 / 1 000 000
- Inheritance: Autosomal dominant
- Age of onset: Adolescent, Adult
- ICD-10: G11.4
- OMIM: 613096
- UMLS: C2936879
- MeSH: -
- GARD: -
- MedDRA: -
Detailed information
Article for general public
Professionals
- Summary information
- Polski (2017, pdf)
- Clinical genetics review
- English (2021)
- Disability factsheet
- Français (2018, pdf)
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
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