A pedigree analysis of deep venous thrombosis caused by rare compound heterozygous PROC mutations combined with a heterozygous THBD mutation

Venous thromboembolism is a common fatal disease that includes pulmonary embolism (PE) and deep vein thrombosis (DVT), and many genetic risk factors are associated with its pathogenesis. We describe a patient with compound heterozygous mutations in PROC combined with a heterozygous mutation in THBD, who was diagnosed with DVT. Genetic sequencing identified three missense mutations in the proband: PROC c.565 C > T (p.R189W), PROC c.1218G > A (p.M406I), and THBD c.1456G > T (p.D486Y), this genotype not previously documented in association with thrombotic disease. His father carried heterozygous mutations of PROC p.R189W and THBD p.D486Y, while his mother and maternal grandfather were heterozygous for PROC p.M406I. These mutations were not detected in other family members.

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Publication Details

Journal
Thrombosis Journal
Published
2025-12-26
DOI
https://doi.org/10.1186/s12959-025-00824-7
Primary Topic
Blood Coagulation and Thrombosis Mechanisms
Type
article
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article

A pedigree analysis of deep venous thrombosis caused by rare compound heterozygous PROC mutations combined with a heterozygous THBD mutation

Rui Tuo, Yang Xiao, Qinglin Mo, Xia Xiao et al.
Thrombosis Journal
Blood Coagulation and Thrombosis Mechanisms
article

A pedigree analysis of deep venous thrombosis caused by rare compound heterozygous PROC mutations combined with a heterozygous THBD mutation

Rui Tuo, Yang Xiao, Qinglin Mo, Xia Xiao, Chun‐Rong Chen, Lixuan Chen, Ying Feng, Chang Su
article en

Abstract

Venous thromboembolism is a common fatal disease that includes pulmonary embolism (PE) and deep vein thrombosis (DVT), and many genetic risk factors are associated with its pathogenesis. We describe a patient with compound heterozygous mutations in PROC combined with a heterozygous mutation in THBD, who was diagnosed with DVT. Genetic sequencing identified three missense mutations in the proband: PROC c.565 C > T (p.R189W), PROC c.1218G > A (p.M406I), and THBD c.1456G > T (p.D486Y), this genotype not previously documented in association with thrombotic disease. His father carried heterozygous mutations of PROC p.R189W and THBD p.D486Y, while his mother and maternal grandfather were heterozygous for PROC p.M406I. These mutations were not detected in other family members.

Thrombosis JournalVol. 24(1)
Guangzhou University of Chinese Medicine (CN), Guangzhou Experimental Station (CN), Second Affiliated Hospital of Guangzhou Medical University (CN), Guangzhou Development Zone Hospital (CN), Jiangmen Central Hospital (CN), Guangzhou Medical University (CN)
Good health and well-being
Openalex Percentile: Top 24%
Blood Coagulation and Thrombosis Mechanisms
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