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Article

Hutchinson-Gilford progeria syndrome with severe skin calcinosis.

Clinical and experimental dermatology - 1 Sept 2007

Nakamura S, Makita Y, Takagi A, Hashimoto Y, Takahashi H, Ishida-Yamamoto A, Iizuka H

Abstract excerpt

We describe a case of Hutchinson-Gilford progeria syndrome (HGPS) with long-term follow-up. A 1-month-old girl with marked sclerodermatous skin changes developed various symptoms of HGPS during follow-up. These included sclerotic skin, pigmentation, skin atrophy with translucent veins, wispy hair and alopecia, nail dystrophy and decreased sweating. Marked skin calcinosis was observed over almost the entire body,...

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Source

Identifiers

PMID: 17459069
DOI: 10.1111/j.1365-2230.2007.02432.x

Genes

LMNA

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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