Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial...

"Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome". Am J Hum Genet. 66 (3): 768–77. doi:10.1086/302831. PMC 1288162...

fuses. The cranial bones are affected as well, similar to Crouzon syndrome and Pfeiffer syndrome. Craniosynostosis occurs when the fetal skull and facial...

Shprintzen-Goldberg syndrome: craniosynostosis with marfanoid habitus and tissue anomalies. Apert syndrome Carpenter syndrome Crouzon syndrome Muenke syndrome Pfeiffer...

neurofibromatosis, LEOPARD syndrome, Crouzon syndrome, Wolf–Hirschhorn syndrome, Andersen–Tawil syndrome, Waardenburg syndrome and cri du chat syndrome, along with piebaldism...

premature fusion of all sutures. It should be differentiated from Crouzon syndrome. Oxycephaly (or acrocephaly) is a form of turricephaly where the head...

Osteoglophonic dysplasia Pfeiffer syndrome Thanatophoric dysplasia, types 1 and 2 Carpenter syndrome Crouzon syndrome Pfeiffer syndrome Thanatophoric dysplasia...

the signs and symptoms of Crouzonodermoskeletal syndrome are similar to those seen with Crouzon syndrome. They include prematurely fused skull bones, which...

syndrome Cri du chat Crigler–Najjar syndrome Crome syndrome Cronkhite–Canada syndrome Cross syndrome Crouzon syndrome Crouzonodermoskeletal syndrome Crush...

of the upper jaw. It is associated with Crouzon syndrome, Angelman syndrome, as well as Fetal alcohol syndrome. It can also be associated with Cleft lip...