Craniosynostosis

Apert Syndrome In nearly all patients with Apert syndrome, the cause is 1 of 2 FGFR2 mutations involving amino acids ........read more

Synonyms of Pfeiffer Syndrome acrocephalosyndactyly, type V ACSV craniofacial-skeletal-dermatologic syndrome Noack syndrome Subdivisions of Pfeiffer Syndrome Pfeiffer syndrome type I ........read more

Crouzon syndrome occurs in about one of every 100,000 births, and also varies considerably in severity. What is Crouzon Syndrome?Crouzon ........read more