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Article

Congenital structural and functional fibrinogen disorders: a primer for internists.

Polish archives of internal medicine - 23 Dec 2019

Undas Anetta, Casini Alessandro

Abstract excerpt

Congenital qualitative and quantitative fibrinogen disorders represent heterogeneous rare abnormalities caused by mutations in one of the 3 genes encoding individual fibrinogen polypeptide chains, located on chromosome 4q28. It is estimated that congenital fibrinogen disorder accounts for 8% of rare coagulation factor deficiencies. Most of congenital fibrinogen disorders are suspected in individuals with bleeding...

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PMID: 31797863
DOI: 10.20452/pamw.15082

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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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