İki kardeşte Crouzon sendromu

Kaynakça (12)

1. Fogh-Andersen P. Craniofacial dysostosis (Crouzon disease) as a dominant hereditary affection. Nord Med. 1943;18:993-6
2. Crouzon LE. Dysostose cranio-faciale hereditaire. Bulletin de la societe des Medecins des Hopitaux de Paris. 1912;33:545-55
3. Panchal J, Uttchin V. Management of craniosynostosis. Plast Reconstr Surg. 2003;111:2032-48
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6. Reardon W, Winter RM, Rutland P, et al. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome. Nature Genet. 1994;8:98-103
7. Carinci F, Pezzetti F, Locci P et al. Apert and Crouzon syndromes: clinical findings, genes and extracellular matrix. J Craniofac Surg. 2005;3:361-6
8. Oliveira CA. Malformações ongênitas da face uma revisão das síndromes mais importantes. Rev Bras Orl. 1982;48:32-8
9. Bowling EL, Burstein FD. Crouzon syndrome. Optometry. 2006;77:217-22
10. Hoefkens MF, Vermeij-Keers C, Vaandrager JM. Crouzon syndrome: phenotypic signs and symptoms of the postnatally expressed subtype. J Craniofac Surg. 2004, 15(2)
11. Gorlin RJ, Cohen MM, Levin LS. Syndromes of the Head and Neck. 3rd edition, Oxford, McGrawHill, 1990
12. Preston RA, Post JC, Keats BJB, et al. A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10. Nat Genet. 1994;7:149-53.