Acrofacial dysostosis Rodriguez type: One of a group of disorders characterized by defective limb and facial development. The Rodriguez type is very rare and primarily involves severe limb and organ malformations. More detailed information about the symptoms, causes, and treatments of Acrofacial dysostosis Rodriguez type is available below.
See full list of 45 symptoms of Acrofacial dysostosis Rodriguez type
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Acrofacial dysostosis Rodriguez 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 Rodriguez type, or a subtype of Acrofacial dysostosis Rodriguez 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 Rodriguez type as a "rare disease".
Source - Orphanet
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