Acrofacial dysostosis, Weyers type: A rare disorder characterized by facial abnormalities and extra digits, nail abnormalities and short limbs. More detailed information about the symptoms, causes, and treatments of Acrofacial dysostosis, Weyers type is available below.
See full list of 11 symptoms of Acrofacial dysostosis, Weyers type
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Acrofacial dysostosis, Weyers type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Acrofacial dysostosis, Weyers type, or a subtype of Acrofacial dysostosis, Weyers 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 Acrofacial dysostosis, Weyers type as a "rare disease".
Source - Orphanet
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