Neurogenic arthrogryposis multiplex congenita (Q85061): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / CURIE | |||
CID11:ID_1594376206 | |||
| Property / CURIE: CID11:ID_1594376206 / rank | |||
Normal rank | |||
Revision as of 10:25, 15 August 2026
Neurogenic arthrogryposis multiplex congenita is a form of arthrogryposis multiplex congenital, characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1594376206 |
||
| English | Neurogenic arthrogryposis multiplex congenita |
Neurogenic arthrogryposis multiplex congenita is a form of arthrogryposis multiplex congenital, characterised by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is caused by neurogenic muscular atrophy. |
Statements
CID11:ID_1594376206
0 references
