Cerebrocostomandibular Syndrome: A rare genetic disorder characterized by a very small jaw, abnormal rib development and a small thorax as well as other abnormalities. More detailed information about the symptoms, causes, and treatments of Cerebrocostomandibular Syndrome is available below.
See full list of 23 symptoms of Cerebrocostomandibular Syndrome
Read more about complications of Cerebrocostomandibular Syndrome.
Research the causes of these diseases that are similar to, or related to, Cerebrocostomandibular Syndrome:
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
See full list of 13 occasional symptoms of Cerebrocostomandibular Syndrome
Medical news articles related to Cerebrocostomandibular Syndrome include:
Source: HealthDay News
Medical research articles related to Cerebrocostomandibular Syndrome include:
Click here to find more evidence-based articles on the TRIP Database
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Visit our research pages for current research about Cerebrocostomandibular Syndrome treatments.
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Mental retardation associated mainly with costovertebral malformations and orofacial defects. Mental defect may not be inherent but rather a consequence of neonatal respiratory distress. - (Source - Diseases Database)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Cerebrocostomandibular Syndrome as a "rare disease".
Source - Orphanet
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