Neurogenic arthrogryposis multiplex congenita (Q85061): Difference between revisions
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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.
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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. |
