Craniotelencephalic dysplasia (medical condition): A very rare syndrome characterized primarily by premature fusion of various skull bones and abnormal brain development.
See also:
Craniotelencephalic dysplasia:
»Introduction: Craniotelencephalic dysplasia
»Symptoms of Craniotelencephalic dysplasia
These medical condition or symptom topics may be relevant to medical information for Craniotelencephalic dysplasia:
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 if affects 1 person per 2,000.
They list Craniotelencephalic dysplasia as a "rare disease".
Source - Orphanet
Craniotelencephalic dysplasia (medical condition): See Craniotelencephalic dysplasia (disease information).
»Introduction: Craniotelencephalic dysplasia
»Symptoms of Craniotelencephalic dysplasia
Source - NIH
Search to find out more about Craniotelencephalic dysplasia:
|
What do you think about the features of this website? Take our user survey and have your say:
Tools & Services:
Medical Articles:
Search Specialists by State and City
By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.
Copyright © 2009 Health Grades Inc. All rights reserved.
