The Sakati Nyhan syndrome (acrocephalosyndactly type III) is an extremely rare type of acrocephalopolysyndactyly.
Its main features include
It was first described by Nadia Awni Sakati, William Leo Nyhan and W K Tisdale in 1971 1.
This article is in need of some more references!
You can make a difference to Radiopaedia.org by adding some relevant ones.
- 1. Sakati N, Nyhan WL, Tisdale WK. A new syndrome with acrocephalopolysyndactyly, cardiac disease, and distinctive defects of the ear, skin, and lower limbs. J. Pediatr. 1971;79 (1): 104-9. - Pubmed citation
Synonyms & Alternative Spellings
|Synonyms or Alternative Spelling||Include in Listings?|
|Acrocephalopolysyndactly type III||✓|
|Sakati Nyhan syndrome||✗|
|Sakati Nyhan Tisdale syndrome||✗|