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Results 1 - 6 of 6 for Familial hemophagocytic lymphohistiocytosis type 1
  1. ... associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5). Blood. 2012 Jun 21;119(25): ...
  2. ... the most common molecular defect in patients with familial hemophagocytic lymphohistiocytosis type 3. Haematologica. 2008 Jul;93(7):1086-90. ...
  3. ... to develop lymphoma, are more likely to develop hemophagocytic lymphohistiocytosis without ... is estimated to occur in about 1 per million males worldwide. XLP2 is less common, ...
  4. ... unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease. Blood. ...
  5. Immune System and Disorders (National Library of Medicine)  
    What is the immune system? Your immune system is a complex network of cells, tissues, and organs. Together they help the body fight infections and other ...
  6. Directory of Transplant Centers (Blood & Marrow Transplant Information Network)  
    ... Fanconi anemia Other Disorders: Glanzmann thrombasthenia Other Disorders: ... - Any - Autologous Allogeneic with related donor ...