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Article

Adult patients with Prader-Willi syndrome: clinical characteristics, life circumstances and growth hormone secretion.

Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society - 1 Apr 2000

Partsch C J, Lämmer C, Gillessen-Kaesbach G, Pankau R

Abstract excerpt

Prader-Willi syndrome is characterized by a typical clinical phenotype and by a complex genetic basis that includes large deletions, uniparental disomy and imprinting mutations of chromosome region 15q11-q13. This report delineates the clinical characteristics, morbidity and growth hormone secret...

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PMID: 10984259
DOI: 10.1016/s1096-6374(00)80015-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-10984259-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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