Distal hereditary motor neuropathy type 3 and type 4 (Q103447): 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 | |||||||||||||||
16 August 2026
| |||||||||||||||
| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 09:12, 17 August 2026
Several kinds have been reported with slowly progressive distal spinal muscular atrophy and autosomal recessive inheritance. Onset of symptoms may develop in infancy or early childhood, or may be delayed into early adulthood. Although relatively benign, ambulation is typically affected. Initially thought to be separate entities due to the variability in age of onset, Distal hereditary motor neuropathy type 3 and 4 have been identified in the same family suggesting a common gene. The responsible gene has been mapped to chromosome 11q13.3.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_91814 |
||
| English | Distal hereditary motor neuropathy type 3 and type 4 |
Several kinds have been reported with slowly progressive distal spinal muscular atrophy and autosomal recessive inheritance. Onset of symptoms may develop in infancy or early childhood, or may be delayed into early adulthood. Although relatively benign, ambulation is typically affected. Initially thought to be separate entities due to the variability in age of onset, Distal hereditary motor neuropathy type 3 and 4 have been identified in the same family suggesting a common gene. The responsible gene has been mapped to chromosome 11q13.3. |
Statements
CID11:ID_91814
0 references
dki-india-ID_91814
0 references
Concluído
0 references
16 August 2026
0 references
