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- W2549530557 endingPage "109" @default.
- W2549530557 startingPage "91" @default.
- W2549530557 abstract "Familial hemophagocytic lymphohistiocytosis (FHL) and Langerhans cell histiocytosis (LCH) are histiocytic diseases that occur most commonly in young children. Improvements in recognition and treatment have been substantial for both diseases in the past decade, although early and late morbidity continue to be major concerns. These two diagnoses behave differently, although the clinical spectra for both diseases are diverse and can lead to confusion and delays in diagnosis and treatment. This article focuses on the clinical and genetic spectrum of FHL as well as the clinical and treatment variations of LCH." @default.
- W2549530557 created "2016-11-30" @default.
- W2549530557 creator A5031468557 @default.
- W2549530557 creator A5045769455 @default.
- W2549530557 creator A5056146847 @default.
- W2549530557 date "2017-02-01" @default.
- W2549530557 modified "2023-10-16" @default.
- W2549530557 title "Usual and Unusual Manifestations of Familial Hemophagocytic Lymphohistiocytosis and Langerhans Cell Histiocytosis" @default.
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