Congenital Antithrombin 3 Deficiency Latest Advances

Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes

Journal: Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

Published: March 16, 2026

Hereditary Antithrombin Deficiency in Pediatric Patients: Pathophysiology, Clinical Features, Diagnosis, and Antithrombin Replacement Therapy.

Journal: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Published: February 18, 2026

Congenital Protein C Deficiency Presenting as Neonatal Purpura Fulminans: A Report of Two Cases.

Journal: Cureus

Published: February 16, 2026

Severe Hemoperitoneum From a Ruptured Ovarian Cyst in a Patient with Antiphospholipid Syndrome and Antithrombin III Deficiency: A Case Report.

Journal: The American journal of case reports

Published: December 06, 2025

Hereditary antithrombin deficiency with recurrent thrombosis caused by a novel SERPINC1 mutation.

Journal: Thrombosis research

Published: November 12, 2025

Systemic Thrombolytic Resistance in Antithrombin III Deficiency Rescued by Catheter-Directed Thrombolysis: A Case Report.

Journal: Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions

Published: October 30, 2025

The unexpected clot: unilateral brachial artery occlusion unmasking antithrombin III deficiency; case report and therapeutic considerations.

Journal: Thrombosis journal

Published: October 18, 2025

Left Renal Artery Thrombosis in a Patient With von Willebrand Disease Type 3 and Factor V Leiden Heterozygosity.

Journal: Cureus

Published: October 07, 2025

Prolonged Neural Block After Lower-Limb Nerve Blocks in a Patient with Inherited Antithrombin III Deficiency: Implications for Regional Anesthesia.

Journal: Local and regional anesthesia

Published: September 02, 2025

Impact of antithrombin III deficiency on clinical outcomes in trauma patients: a systematic review and meta-analysis.

Journal: Journal of thrombosis and thrombolysis

Published: July 30, 2025

Genetic and clinical characterization of two families with severe venous thromboembolism due to nonsense mutations in the SERPINC1 gene.

Journal: Thrombosis journal

Published: July 29, 2025

Clinical and functional characterization of a novel heterozygous mutation c.473T > A (p.Leu158Gln) in the SERPINC1 gene causing recurrent arteriovenous thrombophilia.

Journal: Thrombosis journal

Published: July 15, 2025

Congenital Antithrombin 3 Deficiency Latest Advances

Find the Latest Research About Congenital Antithrombin 3 Deficiency

Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes

Clinical and genetic analysis of two families with combined defect in antithrombin and protein C genes

Hereditary Antithrombin Deficiency in Pediatric Patients: Pathophysiology, Clinical Features, Diagnosis, and Antithrombin Replacement Therapy.

Hereditary Antithrombin Deficiency in Pediatric Patients: Pathophysiology, Clinical Features, Diagnosis, and Antithrombin Replacement Therapy.

Congenital Protein C Deficiency Presenting as Neonatal Purpura Fulminans: A Report of Two Cases.

Congenital Protein C Deficiency Presenting as Neonatal Purpura Fulminans: A Report of Two Cases.

Severe Hemoperitoneum From a Ruptured Ovarian Cyst in a Patient with Antiphospholipid Syndrome and Antithrombin III Deficiency: A Case Report.

Severe Hemoperitoneum From a Ruptured Ovarian Cyst in a Patient with Antiphospholipid Syndrome and Antithrombin III Deficiency: A Case Report.

Hereditary antithrombin deficiency with recurrent thrombosis caused by a novel SERPINC1 mutation.

Hereditary antithrombin deficiency with recurrent thrombosis caused by a novel SERPINC1 mutation.

Systemic Thrombolytic Resistance in Antithrombin III Deficiency Rescued by Catheter-Directed Thrombolysis: A Case Report.

Systemic Thrombolytic Resistance in Antithrombin III Deficiency Rescued by Catheter-Directed Thrombolysis: A Case Report.

The unexpected clot: unilateral brachial artery occlusion unmasking antithrombin III deficiency; case report and therapeutic considerations.

The unexpected clot: unilateral brachial artery occlusion unmasking antithrombin III deficiency; case report and therapeutic considerations.

Left Renal Artery Thrombosis in a Patient With von Willebrand Disease Type 3 and Factor V Leiden Heterozygosity.

Left Renal Artery Thrombosis in a Patient With von Willebrand Disease Type 3 and Factor V Leiden Heterozygosity.

Prolonged Neural Block After Lower-Limb Nerve Blocks in a Patient with Inherited Antithrombin III Deficiency: Implications for Regional Anesthesia.

Prolonged Neural Block After Lower-Limb Nerve Blocks in a Patient with Inherited Antithrombin III Deficiency: Implications for Regional Anesthesia.

Impact of antithrombin III deficiency on clinical outcomes in trauma patients: a systematic review and meta-analysis.

Impact of antithrombin III deficiency on clinical outcomes in trauma patients: a systematic review and meta-analysis.

Genetic and clinical characterization of two families with severe venous thromboembolism due to nonsense mutations in the SERPINC1 gene.

Genetic and clinical characterization of two families with severe venous thromboembolism due to nonsense mutations in the SERPINC1 gene.

Clinical and functional characterization of a novel heterozygous mutation c.473T > A (p.Leu158Gln) in the SERPINC1 gene causing recurrent arteriovenous thrombophilia.

Clinical and functional characterization of a novel heterozygous mutation c.473T > A (p.Leu158Gln) in the SERPINC1 gene causing recurrent arteriovenous thrombophilia.