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Article

[Atypical Werner syndrome: Atypical progeroid syndrome: A case report].

Anales de pediatria (Barcelona, Spain : 2003) - 1 Aug 2010

Barrios Sanjuanelo A, Muñoz Otero C

Abstract excerpt

Progeria is a premature ageing syndrome. Werner Syndrome (WS) is a type of progeria in the adult which includes bilateral juvenile cataracts and cutaneous sclerodermiform changes; it is caused by a mutation if the WRN gene which codes a helicase, a DNA repair enzyme. A case is presented of a patient, a 12 year old girl, with characteristics of WS but with no identifiable mutation in the WRN gene, therefore it was...

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Identifiers

PMID: 20452840
DOI: 10.1016/j.anpedi.2010.02.012

Genes

WRN

Provenance

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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