Familial Hypofibrinogenemia Latest Advances

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: January 18, 2026

Incidence and risk factors of tocilizumab-induced hypofibrinogenemia in patients with thyroid eye disease: a single-center retrospective study.

Journal: Frontiers in endocrinology

Published: January 05, 2026

A novel missense variant (c.1172A>T, p.Asn391Ile) in the gamma chain of fibrinogen causing hypodysfibrinogenemia in an asymptomatic Danish family and review of adjacent variants.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: December 03, 2025

Familial Hypofibrinogenemia Latest Advances

Find the Latest Research About Familial Hypofibrinogenemia

Management of inherited fibrinogen disorder during chemotherapy and allogeneic stem cell transplant.

Management of inherited fibrinogen disorder during chemotherapy and allogeneic stem cell transplant.

An Overview of Dysfibrinogenemia: Pathogenesis, Diagnosis, and Management.

An Overview of Dysfibrinogenemia: Pathogenesis, Diagnosis, and Management.

Individualized Periprocedural Management of Congenital Dysfibrinogenemia during Transvaginal Oocyte Retrieval: A Case Report.

Individualized Periprocedural Management of Congenital Dysfibrinogenemia during Transvaginal Oocyte Retrieval: A Case Report.

Targeting and self-assembling peptides mimic fibrinogen coagulation for alleviating hypofibrinogenemia.

Targeting and self-assembling peptides mimic fibrinogen coagulation for alleviating hypofibrinogenemia.

Identification of genetic variants in the FGB gene associated with congenital hypofibrinogenemia with divergent clinical phenotype.

Identification of genetic variants in the FGB gene associated with congenital hypofibrinogenemia with divergent clinical phenotype.

Repair of severe hand injury by acellular dermal matrix: a rare case of hypofibrinogenaemia resulting in hand injury after haemangioma resection.

Repair of severe hand injury by acellular dermal matrix: a rare case of hypofibrinogenaemia resulting in hand injury after haemangioma resection.

Bleeding from umbilicus in a neonate: exploring aetiologies of a common presentation.

Bleeding from umbilicus in a neonate: exploring aetiologies of a common presentation.

Functional and structural consequences of fibrinogen γ-chain variants associated with thrombotic phenotype in congenital fibrinogen disorders.

Functional and structural consequences of fibrinogen γ-chain variants associated with thrombotic phenotype in congenital fibrinogen disorders.

An exploratory plasma-based functional assay for phenotypic characterization of fibrinolysis in dysfibrinogenemia.

An exploratory plasma-based functional assay for phenotypic characterization of fibrinolysis in dysfibrinogenemia.

Unexpected fibrinogen impairment detected by rotational thromboelastometry in a 76-year-old patient undergoing brain tumor resection: A case report.

Unexpected fibrinogen impairment detected by rotational thromboelastometry in a 76-year-old patient undergoing brain tumor resection: A case report.

Incidence and risk factors of tocilizumab-induced hypofibrinogenemia in patients with thyroid eye disease: a single-center retrospective study.

Incidence and risk factors of tocilizumab-induced hypofibrinogenemia in patients with thyroid eye disease: a single-center retrospective study.

A novel missense variant (c.1172A>T, p.Asn391Ile) in the gamma chain of fibrinogen causing hypodysfibrinogenemia in an asymptomatic Danish family and review of adjacent variants.

A novel missense variant (c.1172A>T, p.Asn391Ile) in the gamma chain of fibrinogen causing hypodysfibrinogenemia in an asymptomatic Danish family and review of adjacent variants.