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
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Research the causes of these diseases that are similar to, or related to, Cerebrocostomandibular Syndrome:
See full list of 13 occasional symptoms of Cerebrocostomandibular Syndrome
Commonly undiagnosed diseases in related medical categories:
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Read more about Misdiagnosis and Cerebrocostomandibular Syndrome
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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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