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Article

Combined congenital dysfibrinogenemia and factor VII deficiency from mutations in the FGB and F7 genes.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jul 2012

Woo Hye In, Park In-Ae, Lee Ki-O, Kim Sun-Hee, Kim Hee-Jin

Abstract excerpt

Dysfibrinogenemia and factor VII (FVII) deficiency are rare congenital coagulopathies. In this report, the authors describe a man with both defects confirmed by molecular genetic tests. The patient was a 51-year-old man referred for prolonged prothrombin time (PT) that had been accidentally detected on preoperative screening. He had no history of bleeding tendency even on occasions of surgery. Routine coagulation...

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Source

Identifiers

PMID: 22576285
DOI: 10.1097/MBC.0b013e32834fa81e

Genes

FGB
FGA
FGG

Variants

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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Combined congenital dysfibrinogenemia and factor VII deficiency from mutations in the FGB and F7 genes.PMID 22576285Read ↗

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