Craniocerebellocardiac dysplasia (medical condition): A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name.
See also:
3C syndrome:
»Introduction: 3C syndrome
»Symptoms of 3C syndrome
These medical condition or symptom topics may be relevant to medical information for Craniocerebellocardiac dysplasia:
Craniocerebellocardiac dysplasia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Craniocerebellocardiac dysplasia, or a subtype of Craniocerebellocardiac dysplasia,
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 Craniocerebellocardiac dysplasia as a "rare disease".
Source - Orphanet
Craniocerebellocardiac dysplasia: Another name for 3C syndrome (or close medical condition association).
»Introduction: 3C syndrome
»Symptoms of 3C syndrome
Some of the symptoms of Craniocerebellocardiac dysplasia incude:
See full list of 33 symptoms of Craniocerebellocardiac dysplasia (3C syndrome)
Source - NIH
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