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Article

Clinical manifestations of the prothrombin G20210A mutation in children: a pediatric coagulation consortium study.

Journal of thrombosis and haemostasis : JTH - 1 May 2003

Young G, Manco-Johnson M, Gill J C, Dimichele D M, Tarantino M D, Abshire T, Nugent D J

Abstract excerpt

The prothrombin G20210A mutation is a common risk factor for thrombosis which increases the risk of deep vein thrombosis, stroke, and fetal loss. There are few publications of its clinical manifestations in children. Our objective was to determine the clinical manifestations of the prothrombin mutation in children. Via survey of pediatric hematologists, we collected data on children with thrombosis and the...

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Identifiers

PMID: 12871361
DOI: 10.1046/j.1538-7836.2003.00116.x

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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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