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Start free with EleplanPure hereditary spastic paraplegia
ORPHA:102012Clinical group
Also called Pure HSP · Pure SPG · Pure familial spastic paraplegia · Uncomplicated HSP · Uncomplicated SPG · Uncomplicated familial spastic paraplegia · Uncomplicated hereditary spastic paraplegia
What it is
Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.
Key facts
- Classified as
- Clinical group
Recorded for the broader condition
- Prevalence
- 1-9 / 100 000Hereditary spastic paraplegia
- Age of onset
- All agesHereditary spastic paraplegia
- Inheritance
- Autosomal dominant, Autosomal recessive, X-linked recessiveHereditary spastic paraplegia
Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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