Craniotelencephalic dysplasia: A very rare syndrome characterized primarily by premature fusion of various skull bones and abnormal brain development. More detailed information about the symptoms, causes, and treatments of Craniotelencephalic dysplasia is available below.
See full list of 10 symptoms of Craniotelencephalic dysplasia
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Read more about causes of Craniotelencephalic dysplasia.
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Read more about Misdiagnosis and Craniotelencephalic dysplasia
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Types of Craniotelencephalic dysplasia
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Craniotelencephalic dysplasia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Craniotelencephalic dysplasia, or a subtype of Craniotelencephalic 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 it affects 1 person per 2,000.
They list Craniotelencephalic dysplasia as a "rare disease".
Source - Orphanet
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