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Article

Otolaryngologic Manifestations of the 22q11.2 Deletion Syndrome

1 Dec 2002

Abstract excerpt

BACKGROUND: The 22q11.2 chromosome deletion syndrome occurs at a frequency of 1 in 4000 live births. Fluorescent in situ hybridization is a reliable means of testing for this genetic abnormality. OBJECTIVE: To describe the otolaryngologic manifestations of the 22q11.2 deletion syndrome to improve recognition and management of these disorders. PATIENTS AND DESIGN: A retrospective medical record review of 102...

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PMID: 12479730
DOI: 10.1001/archotol.128.12.1408

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