Arthrogryposis multiplex congenita type 2B: A form of distal arthrogryposis (joint contractures in ends of limbs) that also involves craniofacial abnormalities. More detailed information about the symptoms, causes, and treatments of Arthrogryposis multiplex congenita type 2B is available below.
See full list of 30 symptoms of Arthrogryposis multiplex congenita type 2B
Read more about causes of Arthrogryposis multiplex congenita type 2B.
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Read more about Misdiagnosis and Arthrogryposis multiplex congenita type 2B
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Arthrogryposis multiplex congenita type 2B 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 type 2B, or a subtype of Arthrogryposis multiplex congenita type 2B,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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