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CASE REPORT
Year : 2013  |  Volume : 6  |  Issue : 2  |  Page : 255-258

Familial haemophagocytic lymphohistiocytosis


Department of Pediatrics, Hatta Hospital, Hatta, United Arab Emirates

Correspondence Address:
Ammar MH Shehadeh
Department of Pediatrics, Hatta Hospital, Hatta
United Arab Emirates
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Source of Support: None, Conflict of Interest: None


DOI: 10.7707/hmj.v6i2.240

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Haemophagocytic lymphohistiocytosis (HLH) is a rare, but potentially fatal, disease that occurs when normal histiocytes and lymphocytes become overactive and commonly occurs in infancy. Two forms of the disease have been described: primary and secondary. This article reports twins who were less than 2 years old at the time of presentation and who had clinical symptoms of primary (familial) HLH, which was diagnosed by a contributory pathological bone marrow test.


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