Cerebrofaciothoracic dysplasia: a new family.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 1640432.
- Also identified by PMC identifier 1016029.
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Abstract
We describe two brothers, born to consanguineous parents, who had facial dysmorphism, complex anomalies of the vertebrae and ribs, enlarged cerebral ventricles and septum pellucidum, mental retardation, and affable behaviour. The features are similar to those previously described in three unrelated children and may represent new cases of cerebrofaciothoracic dysplasia.
Medical subject headings
- Abnormalities, Multiple
- Face
- Skull
- Thorax