Oculomelic amyoplasia (medical condition): A rare genetic disorder characterized by limb contractures (tightening of muscles which limits movement) from birth and eye abnormalities.
See also:
Oculomelic amyoplasia:
»Introduction: Oculomelic amyoplasia
»Symptoms of Oculomelic amyoplasia
These medical condition or symptom topics may be relevant to medical information for Oculomelic amyoplasia:
Oculomelic amyoplasia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Oculomelic amyoplasia, or a subtype of Oculomelic amyoplasia,
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 if affects 1 person per 2,000.
They list Oculomelic amyoplasia as a "rare disease".
Source - Orphanet
Oculomelic amyoplasia (medical condition): See Oculomelic amyoplasia (disease information).
»Introduction: Oculomelic amyoplasia
»Symptoms of Oculomelic amyoplasia
Source - NIH
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