Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defects.
case_report · Level V
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- Record sourced from PubMed, PMID 1404297.
- Also identified by PMC identifier 1016100.
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Abstract
We describe a two generation family with variable ulnar and radial ray reduction and midline craniofacial abnormalities. The features suggest a diagnosis of Weyers' ulnar ray/oligodactyly syndrome originally described in two isolated cases. Syndromes of ulnar ray reduction are briefly reviewed and the relationship between limb bud and midline development discussed.
Medical subject headings
- Abnormalities, Multiple
- Fingers
- Hand Deformities, Congenital
- Radius
- Tooth Abnormalities
- Ulna