Massa-Casaer-Ceulemans syndrome: A very rare syndrome characterized mainly by abnormal brain development (lissencephaly - smooth brain) and multiple joint contractures at birth. More detailed information about the symptoms, causes, and treatments of Massa-Casaer-Ceulemans syndrome is available below.
See full list of 7 symptoms of Massa-Casaer-Ceulemans syndrome
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Types of Massa-Casaer-Ceulemans syndrome
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Massa-Casaer-Ceulemans syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Massa-Casaer-Ceulemans syndrome, or a subtype of Massa-Casaer-Ceulemans syndrome,
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 Massa-Casaer-Ceulemans syndrome as a "rare disease".
Source - Orphanet
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