Spastic paraplegia 14: Difference between revisions
From WikiMD's Wellness Encyclopedia
Created page with "== '''Alternate names''' == SPG14 == '''Definition''' == Autosomal recessive spastic paraplegia type 14 is a rare, complex hereditary spastic paraplegia characterized by..." Tag: visualeditor-wikitext |
CSV import |
||
| Line 7: | Line 7: | ||
{{rarediseases}} | {{rarediseases}} | ||
{{stb2}} | {{stb2}} | ||
__NOINDEX__ | |||
Latest revision as of 08:13, 4 February 2025
Alternate names
SPG14
Definition
Autosomal recessive spastic paraplegia type 14 is a rare, complex hereditary spastic paraplegia characterized by adulthood-onset of slowly progressive spastic paraplegia of lower limbs presenting with spastic gait, hyperreflexia, and mild lower limb hypertonicity associated with mild intellectual disability, visual agnosia, short and long-term memory deficiency and mild distal motor neuropathy. Bilateral pes cavus and extensor plantar responses are also associated.
NIH genetic and rare disease info
Spastic paraplegia 14 is a rare disease.
| Rare and genetic diseases | ||||||
|---|---|---|---|---|---|---|
|
Rare diseases - Spastic paraplegia 14
|
Resources
| Additional resources | ||
|---|---|---|
|
Spastic paraplegia 14
|
<html><link rel="canonical" href="https://wikimd.com/wiki/Spastic+paraplegia+14">
<meta name=”viewport” content=”width=device-width, initial-scale=1″>
</html>
