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Article

The oro-dental phenotype in Prader-Willi syndrome: a survey of 15 patients.

International journal of paediatric dentistry - 1 Jan 2008

Bailleul-Forestier Isabelle, Verhaeghe Veroniek, Fryns Jean-Pierre, Vinckier Frans, Declerck Dominique, Vogels Annick

Abstract excerpt

BACKGROUND: Prader-Willi syndrome (PWS) is a rare disorder caused by genetic defects in certain regions of chromosome 15q11-13. It is characterized by severe neonatal hypotonia and feeding problems, childhood-onset hyperphagia and obesity, short stature, facial dysmorphy, hypogonadism, learning and behavioural difficulties, and dental abnormalities. AIM: To describe the oro-dental phenotypic spectrum of patients...

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Identifiers

PMID: 18086025
DOI: 10.1111/j.1365-263X.2007.00857.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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