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disease > genetic disease > hereditary disease > Crouzon disease
disease > congenital disease > malformation > dysostosis > Crouzon disease
disease > diseases of the osteoarticular system > dysostosis > Crouzon disease

Terme préférentiel

Crouzon disease  

Définition

  • Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. (Wikipedia)

Concept générique

Traductions

URI

http://data.loterre.fr/ark:/67375/VH8-VRW6TJKT-W

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