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Article

Can the phenotype of inherited fibrinogen disorders be predicted?

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Sept 2016

Casini A, de Moerloose P

Abstract excerpt

Congenital fibrinogen disorders are rare diseases affecting either the quantity (afibrinogenaemia and hypofibrinogenaemia) or the quality (dysfibrinogenaemia) or both (hypodysfibrinogenaemia) of fibrinogen. In addition to bleeding, unexpected thrombosis, spontaneous spleen ruptures, painful bone cysts and intrahepatic inclusions can complicate the clinical course of patients with quantitative fibrinogen...

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Identifiers

PMID: 27293018
DOI: 10.1111/hae.12967

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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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