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Article

Subclinical dysphagia in persons with Prader-Willi syndrome.

American journal of medical genetics. Part A - 1 Feb 2017

Gross Roxann Diez, Gisser Ronit, Cherpes Gregory, Hartman Katie, Maheshwary Rishi

Abstract excerpt

Prader-Willi Syndrome (PWS) is caused by a genetic imprinting abnormality resulting from the lack of expression of the paternal genes at 15q11-q13. Intellectual disability, low muscle tone, and life-threatening hyperphagia are hallmarks of the phenotype. The need for the Heimlich maneuver, death from choking, and pulmonary infection occur in a disproportionally high number of persons with PWS. The widely held...

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Identifiers

PMID: 27759943
DOI: 10.1002/ajmg.a.38015

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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