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Fig. 1 | Thrombosis Journal

Fig. 1

From: Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency

Fig. 1

(a–b) Two pedigree profiles of hereditary antithrombin deficiency. (c) Computed tomographic angiography (CTA) findings of the small bowel mesenteric vessels in proband (III1) of Pedigree A showed thrombosis in the inferior vena cava, left common iliac vein, external iliac vein, and left external iliac vein. (d–e) Digital subtraction angiography findings of the proband (III1) in Pedigree B showed thrombosis of the right superficial femoral vein-common femoral vein and distal right external iliac vein. (f) A heterozygous mutation SERPINC1 c.1377delC: p.Asn460Thrfs*20 was found in the proband of Pedigree A (III1). (g) Wild-type at c.1377C. (h) A heterozygous mutation SERPINC1 c.685C > T: p. (Arg229*) was found in the proband of Pedigree B. (i) Wild-type of c.685C

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Thrombosis Journal

ISSN: 1477-9560

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