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Article

Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome.

International journal of pediatric otorhinolaryngology - 1 Dec 2012

Lay-Son Guillermo, Palomares Mirta, Guzman M Luisa, Vasquez Marcos, Puga Alonso, Repetto Gabriela M

Abstract excerpt

OBJECTIVE: Chromosome 22q11 microdeletion syndrome (del22q11) is the most frequent microdeletion syndrome in humans, with an estimated incidence of 1/4000. It is recognized as a common identifiable cause of cleft palate. We characterized palatal abnormalities in a large cohort of Chilean patients with del22q11. METHODS: Patients with the deletion were evaluated by geneticists and speech pathologists, including...

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Identifiers

PMID: 22939891
DOI: 10.1016/j.ijporl.2012.08.010

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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