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Article

Laryngeal atresia type III (glottic web) with 22q11.2 microdeletion: Report of three patients

16 May 1997

Abstract excerpt

The clinical manifestations of patients with a 22q11.2 deletion are highly variable and mainly include developmental defects of structures derived from the third and fourth pharyngeal pouches. Laryngeal atresia has occasionally been reported in DiGeorge syndrome as well as in velo-cardio-facial syndrome. We observed three patients with type III laryngeal atresia (glottic web) and 22q11.2 microdeletion. One...

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Identifiers

PMID: 9128930
DOI: 10.1002/(sici)1096-8628(19970516)70:2<130::aid-ajmg5>3.0.co;2-1

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