Pfeiffer syndrome

Pfeiffer syndrome (PS) is a common form of acrocephalosyndactyly, a group of inherited congenital malformation disorders, characterized by variable degrees of bicoronal craniosynostosis, variable hand and foot malformations and various other associated manifestations.

Also known as: ACS5, Pfeiffer syndrome, acrocephalosyndactyly type 5, acrocephalosyndactyly type V, type V Acrocephalosyndactyly, ACS 5, Noack syndrome, Pfeiffer type acrocephalosyndactyly

41 clinical trials for this condition and its sub-types.