Craniofacial conodysplasia.
case_report · Level V
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- Record sourced from PubMed, PMID 7593576.
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Abstract
A family with dominant inheritance of a previously unreported syndrome of craniofacial dysplasia and cone-shaped physes of the hands and feet is described. Hydrocephalus and spinal cord compression at the craniocervical junction causes neurological complications and mimics cerebral palsy. Early diagnosis and treatment may prevent progression of neurological changes.
Medical subject headings
- Bone Diseases, Developmental
- Epiphyses
- Facial Bones
- Hand Deformities, Congenital
- Skull
Anatomy
- hand