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Article

The transition between the phenotypes of Prader-Willi syndrome during infancy and early childhood.

Developmental medicine and child neurology - 1 Jun 2010

Butler Jill V, Whittington Joyce E, Holland Anthony J, McAllister Catherine J, Goldstone Anthony P

Abstract excerpt

AIM: Prader-Willi syndrome (PWS) is a genetic disorder historically characterized by two phenotypic stages. The early phenotype in infants is associated with hypotonia, poor suck, and failure to thrive. In later childhood, PWS is associated with intellectual disability, hyperphagia, as well as gr...

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PMID: 20041936
DOI: 10.1111/j.1469-8749.2009.03530.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20041936-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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