A case of congenital TTP presenting with microganiopathy in adulthood
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,Molecular Biology
Link
http://link.springer.com/content/pdf/10.1186/2052-1839-14-16.pdf
Reference9 articles.
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2. Upshaw JD: Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia. New Engl J Med. 1978, 298: 1350-1352. 10.1056/NEJM197806152982407.
3. Moake JL, Rudy CK, Troll JH, Weinstein MJ, Colannino NM, Azocar J, Seder RH, Hong SL, Deykin D: Unusually large plasma factor VIII: von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. New Engl J Med. 1982, 307: 1432-1435. 10.1056/NEJM198212023072306.
4. Furlan M, Robles R, Solenthaler M, Wassmer M, Sandoz P, Lämmle B: Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood. 1997, 89: 3097-3103.
5. Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V, Stabler SP, Sabio H, Bouhassira EE, Upshaw JD, Ginsburg D, Tsai HM: Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 2001, 413: 488-494. 10.1038/35097008.
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