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Familial hemophagocytic lymphohistiocytosis in a newborn presenting with recurrent fever and thrombocytopenia

  
@article{PM5009,
	author = {Rong Yin and Hongsheng Wang and Zhihua Li and Yun Cao and Lin Yang and Huijun Wang and Bingbing Wu and Christopher Dandoy and Erika L. Stalets and Blachy J. Dávila Saldaña and Laishuan Wang and Wenhao Zhou},
	title = {Familial hemophagocytic lymphohistiocytosis in a newborn presenting with recurrent fever and thrombocytopenia},
	journal = {Pediatric Medicine},
	volume = {2},
	number = {0},
	year = {2019},
	keywords = {},
	abstract = {Familial hemophagocytic lymphohistiocytosis (HLH) is a rare and potentially fatal disease with major difficulties of diagnosis and treatment, especially in the neonatal period (1-3). Early diagnosis and early treatment of HLH improves patients’ outcomes. Herein, we present a Familial HLH case and discuss the differential diagnosis and the cutting edge opinions of treatment by the experts in this area.},
	url = {http://pm.amegroups.com/article/view/5009}
}