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Familial Hemophagocytic Lymphohistiocytosis - Primary Hemophagocytic Lymphohistiocytosis

HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, no. 2 (1998): 417-+

Cited: 295|Views7

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JPER neonatology perinatology maternal-fetal prematureMore(5+)

Abstract

Hemophagocytic lymphohistiocytosis represents a spectrum of pathogenetically different diseases including the rapidly fatal autosomal recessive disease of familial hemophagocytic lymphohistiocytosis (FHL). The onset is usually during the first years of life with fever, cytopenia, and hepatosplenomegaly. Neurologic symptoms may supervene. ...More

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