PROTEIN C DEFICIENCY AND PORTAL THROMBOSIS IN LIVER TRANSPLANTATION IN CHILDREN

The Lancet ◽  
1988 ◽  
Vol 332 (8617) ◽  
pp. 924-927 ◽  
Author(s):  
P.L. Harper ◽  
R.J. Luddington ◽  
R.W. Carrell ◽  
N. Barnes ◽  
P.F. Edgar ◽  
...  
1995 ◽  
Vol 8 (4) ◽  
pp. 307-311 ◽  
Author(s):  
M. Cransac ◽  
J. Carles ◽  
P.-H. Bernard ◽  
P. Malavialle ◽  
G. Freyburger ◽  
...  

2015 ◽  
Vol 19 (3) ◽  
pp. E70-E74 ◽  
Author(s):  
Masatoshi Matsunami ◽  
Akira Ishiguro ◽  
Akinari Fukuda ◽  
Kengo Sasaki ◽  
Hajime Uchida ◽  
...  

2017 ◽  
Vol 64 (10) ◽  
pp. e26521 ◽  
Author(s):  
Yi-Ting Yeh ◽  
Hsiu-Ju Yen ◽  
Niang-Cheng Lin ◽  
Kuo-Chiang Wang ◽  
Hsin-Lin Tsai ◽  
...  

The Lancet ◽  
1989 ◽  
Vol 333 (8629) ◽  
pp. 102-103 ◽  
Author(s):  
M.D Stringer ◽  
E Melissari ◽  
V.V Kakkar ◽  
K.C Tan

2018 ◽  
Vol 93 (3) ◽  
pp. 462-466
Author(s):  
Alexander A. Boucher ◽  
Lori Luchtman-Jones ◽  
Jaimie D. Nathan ◽  
Joseph S. Palumbo

2001 ◽  
Vol 40 (5) ◽  
pp. 671
Author(s):  
Mi Ae Cheong ◽  
Kyu Sam Hwang ◽  
Kyu Taek Choi ◽  
Yoon Choi ◽  
Eun Ju Lee ◽  
...  

1988 ◽  
Vol 59 (01) ◽  
pp. 018-022 ◽  
Author(s):  
C L Gladson ◽  
I Scharrer ◽  
V Hach ◽  
K H Beck ◽  
J H Griffin

SummaryThe frequency of heterozygous protein C and protein S deficiency, detected by measuring total plasma antigen, in a group (n = 141) of young unrelated patients (<45 years old) with venous thrombotic disease was studied and compared to that of antithrombin III, fibrinogen, and plasminogen deficiencies. Among 91 patients not receiving oral anticoagulants, six had low protein S antigen levels and one had a low protein C antigen level. Among 50 patients receiving oral anticoagulant therapy, abnormally low ratios of protein S or C to other vitamin K-dependent factors were presented by one patient for protein S and five for protein C. Thus, heterozygous Type I protein S deficiency appeared in seven of 141 patients (5%) and heterozygous Type I protein C deficiency in six of 141 patients (4%). Eleven of thirteen deficient patients had recurrent venous thrombosis. In this group of 141 patients, 1% had an identifiable fibrinogen abnormality, 2% a plasminogen abnormality, and 3% an antithrombin III deficiency. Thus, among the known plasma protein deficiencies associated with venous thrombosis, protein S and protein C. deficiencies (9%) emerge as the leading identifiable associated abnormalities.


1990 ◽  
Vol 64 (02) ◽  
pp. 239-244 ◽  
Author(s):  
P H Reitsma ◽  
W te Lintel Hekkert ◽  
E Koenhen ◽  
P A van der Velden ◽  
C F Allaart ◽  
...  

SummaryScreening of restriction erzyme digested DNA from normal and protein C deficient individuals with a variety of probes derived from the protein C locus has revealed the existence of two neutral MspI polymorphism. One polymorphism (MI), which is located ≈7 kb upstream of the protein C gene, has allelic frequencies of 69 and 31%, and was used to exclude extensive gene deletions as a likely cause of type I protein C deficiency in 50% of cases in a panel of 22 families. Furtherrnore, the same polymorphism has been used in 5 doubly affected individuals establishing compound heterozygosity in 3 of these.The second, intragenic, polymorphism (MII) has allelic frequencies of 99 and 1% in the normal population. The frequency of the rare allele of this RFLP was with 7% much higher in a panel of 22 Dutch families with protein C deficiency. Interestingly, in all three probands that were heterozygous for MII the rare allele of MII coincided with a point mutation that leads to a stop codon in amino acid position 306 of the protein C coding sequence. This mutation may account for 14% of the protein C deficient individuals in The Netherlands.


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