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Article

Hutchinson-Gilford progeria syndrome.

Handbook of clinical neurology - 1 Jan 2015

Ullrich Nicole J, Gordon Leslie B

Abstract excerpt

Hutchinson-Gilford progeria syndrome (HGPS) is an extremely rare, uniformly fatal, segmental "premature aging" disease in which children exhibit phenotypes that may give us insights into the aging process at both the cellular and organismal levels. Initial presentation in early childhood is primarily based on growth and dermatologic findings. Primary morbidity and mortality for children with HGPS is from...

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PMID: 26564085
DOI: 10.1016/B978-0-444-62702-5.00018-4

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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