[MIM 101120]

(Sakati syndrome)

Very rare syndrome belonging to the group of the A.C.P.S. (acrocephalopolysyndactylies) and identified as ACPS type 3.

Outside the classical anomalies of the ACPS (acrocephaly, craniostenosis, hand and foot syndactylies or polydactylies), some other anomalies are associated:

-  lower limb bones anomalies

-  cardiac defects

-  ear and skin anomalies

Anesthetic implications: 

difficult intubation, risk of increased intracranial pressure; echocardiography

Updated: August 2016