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Article

Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management.

Journal of thrombosis and haemostasis : JTH - 1 Jun 2015

Casini A, Neerman-Arbez M, Ariëns R A, de Moerloose P

Abstract excerpt

Congenital dysfibrinogenemia is a qualitative congenital fibrinogen disorder characterized by normal antigen levels of a dysfunctional fibrinogen. The diagnosis is usually based on discrepancies between fibrinogen activity and antigen levels, but could require more specialized techniques for the assessment of fibrinogen function, owing to some limitations in routine assays. Molecular abnormalities, which are...

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Source

Identifiers

PMID: 25816717
DOI: 10.1111/jth.12916

Genes

FGA
FGG

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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