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Completely cartilaginous trachea in a child with Crouzon syndrome.

作者信息

Devine P, Bhan I, Feingold M, Leonidas J C, Wolpert S M

出版信息

Am J Dis Child. 1984 Jan;138(1):40-3. doi: 10.1001/archpedi.1984.02140390032010.

DOI:10.1001/archpedi.1984.02140390032010
PMID:6546324
Abstract

We describe a patient with Crouzon syndrome and congenital tracheal stenosis. The trachea lacked rings and was completely cartilaginous, making it rigid and narrow. The respiratory difficulties that are present in patients with Crouzon syndrome have been ascribed to the nasal or choanal defects that are associated with this condition. However, the presence of congenital tracheobronchial abnormalities as a cause of respiratory problems has not been widely investigated. Congenital tracheal stenosis may occur as an isolated defect or as one of many other congenital defects. In patients with Crouzon syndrome who have recurrent respiratory problems, congenital tracheal or bronchial defects should be considered since surgical intervention may correct the defect.

摘要

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