hereditary spastic paraplegia (Q657516)
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genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs
- HSMN V
- familial spastic paraplegia
- Strümpell-Lorrain disease
- French settlement disease
- Strumpell-Lorrain disease
- hereditary spastic paraparesis
- FSP
- HSP
- SPG
- StrC<mpell-Lorrain disease
- Familial spastic paraparesis
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hereditary spastic paraplegia |
genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs |
|
Statements
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334.1
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C140267
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Hereditary spastic paraplegia
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Identifiers
Spastic Paraplegia, Hereditary
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Sitelinks
Wikipedia(14 entries)
- arwiki شلل نصفي تشنجي موروث
- cawiki Paraplegia espàstica hereditària
- dawiki Arvelig spastisk paraplegi
- dewiki Spastische Paraplegie
- enwiki Hereditary spastic paraplegia
- eswiki Síndrome de Strumpell Lorrain
- frwiki Paraplégie spastique familiale
- itwiki Paraparesi spastica ereditaria
- nlwiki Hereditaire spastische paraparese
- plwiki Choroba Strümplla
- ptwiki Paraparesia espástica familiar
- ruwiki Спастическая спинальная параплегия
- uzwiki Umurtqa spastik paraplegiyasi
- zhwiki 遺傳性痙攣性下半身麻痺
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Wikiquote(0 entries)
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Wikiversity(0 entries)
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Wiktionary(0 entries)
Multilingual sites(1 entry)
- commonswiki Category:Hereditary spastic paraplegia