Rare Bleeding and Clotting Disorders
Special Edition of Haemophilia
November 2008
Foreword
Amy D. Shapiro, Donna M. DiMichele, W. Keith Hoots, Marion A. Koerper, Marilyn J. Manco-Johnson, Diane J. Nugent, Flora Peyvandi, Mark W. Skinner
Rare Inherited Disorders of Fibrinogen
Suchitra S. Acharya and Donna M. DiMichele
Abnormalities of Prothrombin: A Review of the Pathophysiology, Diagnosis, and Treatment
Shannon L. Meeks and Thomas C. Abshire
Factor V Deficiency: A Concise Review
James N. Huang and Marion A. Koerper
Factor IV Deficiency: Defining the Clinical Picture and Optimizing Therapeutic Options
Mario Lapecorella and Guglielmo Mariani
Diagnosis and Treatment of Inherited Factor X Deficiency
Deborah L. Brown and Peter A. Kouides
Factor XI Deficiency
Keith Gomez and Paula Bolton-Maggs
Factor XIII Deficiency
Loan Hsieh and Diane Nugent
Combined FV and FVIII Deficiency
Marta Spreafico and Flora Peyvandi
Familial Deficiency of Vitamin K–Dependent Clotting Factors
Brent W. Weston and Paul E. Monahan
Protein C Deficiency
Neil A. Goldenberg and Marilyn J. Manco-Johnson
Protein S Deficiency: A Clinical Perspective
Min Ki ten Kate and Jan van der Meer
Inherited Antithrombin Deficiency: A Review
Mrinal M. Patnaik and Stephan Moll
Platelet Function Defects
David Simon, Thomas Kunicki, and Diane Nugent
α2-Antiplasmin and Its Deficiency: Fibrinolysis Out of Balance
Shannon L. Carpenter and Prasad Mathew
Plasminogen Activator Inhibitor Type 1 Deficiency
Rakesh Mehta and Amy D. Shapiro
Plasminogen Deficiency
Rakesh Mehta and Amy D. Shapiro
Hereditary Hemorrhagic Telangiectasia
Anjali A. Sharathkumar and Amy D. Shapiro
