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Familial hemophagocytic lymphohistiocytosis type 1
- ... associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5). Blood. 2012 Jun 21;119(25): ...
- ... the most common molecular defect in patients with familial hemophagocytic lymphohistiocytosis type 3. Haematologica. 2008 Jul;93(7):1086-90. ...
- ... 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, ...
- ... unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease. Blood. ...
- 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 ...