Pfeiffer syndrome

MONDO:0007043

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

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