Neurogenic arthrogryposis multiplex congenita is a form of arthrogryposis multiplex congenita characterized by congenital immobility of the limbs with fixation of multiple joints and muscle wasting. This condition is secondary to neurogenic muscular atrophy.
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prenatal-onset spinal muscular atrophy with congenital bone fractures
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adducted thumbs-arthrogryposis syndrome, Christian type
MONDO:0008724
fetal akinesia deformation sequence
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arthrogryposis multiplex congenita-whistling face syndrome
MONDO:0008825
arthrogryposis-hyperkeratosis syndrome, lethal form
MONDO:0008826
multiple pterygium-malignant hyperthermia syndrome
MONDO:0009012