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Abstract

Editorial on Pfeiffer Syndrome

Pfeiffer syndrome is a rare genetic disorder characterized by premature fusion of certain skull bones and other birth defects in the hands and feet. The abnormality of the skull bones causes changes in the shape of the face and head. Most affected individuals also have differences to their midface and conductive hearing loss. This syndrome also affects bones in the hands and feet. It’s also referred to as acrocephalosyndactyly type V, ACSV, craniofacial-skeletal-dermatologic syndrome, and Noack syndrome [1-3].


Author(s):

Sophia Roberts*



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