Autosomal dominant spastic paraplegia type 19 (Q100872): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (2 intermediate revisions by the same user not shown) | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 17:39, 16 August 2026
Autosomal dominant spastic paraplegia associated with SPG19 gene that presents with slowly progressive spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction, and mild sensory and motor peripheral neuropathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1020508875 |
||
| English | Autosomal dominant spastic paraplegia type 19 |
Autosomal dominant spastic paraplegia associated with SPG19 gene that presents with slowly progressive spastic paraplegia presenting in adulthood with spastic gait, lower limb hyperreflexia, extensor plantar responses, bladder dysfunction, and mild sensory and motor peripheral neuropathy. |
Statements
CID11:ID_1020508875
0 references
dki-india-ID_1020508875
0 references
Concluído
0 references
15 August 2026
0 references
