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. 2011 Nov 14;17(42):4704–4710. doi: 10.3748/wjg.v17.i42.4704

Table 3.

Relationship between gender and etiology in patients with Budd-Chiari syndrome (n = 94)

Etiology Gender n (%) χ² P value Sig
Male Female
PC deficiency + 1 (2.90) 3 (5.20)   1 NS
PS deficiency + 1 (2.90) 0 (0.00) 0.38 NS
AT III deficiency + 2 (5.70) 2 (3.40) 0.63 NS
FVLM Homozygous 5 (20.80) 5 (12.50) 1.77 0.18 NS
Heterozygous 6 (25.00) 18 (45.00)
PGM Homozygous 0 (0.00) 1 (2.60) 1.54 0.21 NS
Heterozygous 0 (0.00) 2 (5.10)
MTHFR Homozygous 6 (28.60) 2 (5.10) 8.41 0.01 HS
Heterozygous 9 (42.90) 14 (35.90)
JAK2 (MPD) + 6 (28.60) 12 (29.30) 0.003 0.95 NS
Primary APA + 5 (13.90) 11 (19.00) 0.4 0.52 NS
Secondary APA + 1 (2.80) 10 (17.20) 0.05 S
Behçet’s disease + 11 (30.60) 1 (1.70) < 0.001 VHS
PNH + 1 (2.80) 1 (1.70) 1 NS

Sig: Significance; NS: Not significant; S: Significant; HS: Highly significant; VHS: Very highly significant; PC: Protein C; PS: Protein S; AT: Antithrombin; FVLM: Factor V Leiden mutation; PGM: Prothrombin gene mutation; MTHFR: Methylene tetrahydrofolate reductase; JAK2: Janus tyrosine kinase-2; MPD: Myeloproliferative disorder; APA: Antiphospholipid antibody syndrome; PNH: Paroxysmal nocturnal hemoglobinuria.