Neurogenic arthrogryposis multiplex congenita (Q85061): Difference between revisions
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Latest 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 |
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| default for all languages | ID_1594376206 |
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| 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. |
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CID11:ID_1594376206
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dki-india-ID_1594376206
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Concluído
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13 August 2026
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