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Article

Prader-Willi Syndrome: A spectrum of anatomical and clinical features.

Clinical anatomy (New York, N.Y.) - 1 Jul 2016

Hurren Bradley J, Flack Natasha A M S

Abstract excerpt

Prader-Willi Syndrome (PWS) is estimated to affect 400,000 people worldwide. First described clinically in 1956, PWS is now known to be a result of a genetic mutation, involving Chromosome 15. The phenotypical appearance of individuals with the syndrome follows a similar developmental course. During infancy, universal hypotonia accompanied by feeding problems, hypogonadism, and dolichocephaly are evident....

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Identifiers

PMID: 26749552
DOI: 10.1002/ca.22686

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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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