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Article

Hutchinson-Gilford progeria syndrome caused by an LMNA mutation: a case report.

Pediatric dermatology - 1 Jan 2000

Chu Yan, Xu Zi-Gang, Xu Zhe, Ma Lin

Abstract excerpt

Hutchinson-Gilford progeria syndrome is a rare genetic disorder characterized by premature aging of the skin, bones, heart, and blood vessels. We report a 6-year-old boy who was born at full term but presented with scleroderma-like appearance at 1 month of age and gradually developed clinical manifestations of progeria. He had characteristic facial features of prominent eyes, scalp, and leg veins; loss of scalp...

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Source

Identifiers

PMID: 25556323
DOI: 10.1111/pde.12406

Genes

LMNA

Variants

Provenance

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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Hutchinson-Gilford progeria syndrome caused by an LMNA mutation: a case report.PMID 25556323Read ↗

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