Sakati-Nyhan syndrome
The Sakati-Nyhan syndrome, also known as Sakati-Nyhan-Tisdale syndrome or acrocephalosyndactly type III, is an extremely rare type of acrocephalopolysyndactyly.
Its main features include:
- craniofacial defects
- congenital limb abnormalities
- congenital heart defects
History and etymology
It was first described by Nadia Awni Sakati, William Leo Nyhan and W K Tisdale in 1971 .
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