Sakati–Nyhan–Tisdale syndrome
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Sakati–Nyhan–Tisdale syndrome,[1] is a rare genetic disorder that has been associated with abnormalities in the bones of the legs, congenital heart defects and craniofacial defects. The syndrome belongs to a group of rare genetic disorders known as acrocephalopolysyndactyly or ACPS, for short.[2]
Quick Facts Other names, Specialty ...
Sakati–Nyhan–Tisdale syndrome | |
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Other names | Acrocephalopolysyndactyly type III |
This condition is inherited in an autosomal dominant manner | |
Specialty | Medical genetics |
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