Arthrogryposis multiplex congenita neurogenic type: A rare non-progressive syndrome characterized by congenital contractures that originates from a nerve problem (spinal motor neuron depletion). More detailed information about the symptoms, causes, and treatments of Arthrogryposis multiplex congenita neurogenic type is available below.
See full list of 17 symptoms of Arthrogryposis multiplex congenita neurogenic type
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Read more about causes of Arthrogryposis multiplex congenita neurogenic type.
See full list of 7 occasional symptoms of Arthrogryposis multiplex congenita neurogenic type
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Arthrogryposis multiplex congenita neurogenic type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Arthrogryposis multiplex congenita neurogenic type, or a subtype of Arthrogryposis multiplex congenita neurogenic type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Arthrogryposis multiplex congenita neurogenic type as a "rare disease".
Source - Orphanet
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