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  5. Familial hemophagocytic lymphohistiocytosis type 2 in a female Chinese neonate:A case report and rev

Familial hemophagocytic lymphohistiocytosis type 2 in a female Chinese neonate:A case report and rev

来源 :世界临床病例杂志 | 被引量 : 0次 | 上传用户：wrx5428167
【摘 要】
：
BACKGROUND Familial hemophagocytic lymphohistiocytosis type 2(FHL2)is a rare genetic disorder presenting with fever,hepatosplenomegaly,and pancytopenia secondary to perforin-1(PRF1)mutation.FLH2 has been described in Chinese but usually presents after 1 y
【作 者】
：
Shao-Hua Bi Liang-Liang Jiang Li-Ying Dai Li-Li Wang Guang-Hui Liu Ru-Jeng Teng 
【机 构】
：
DivisionofNeonatology,DepartmentofNeonatology,DepartmentofPediatricNeurology,DepartmentofPediatrics
【出 处】
：
世界临床病例杂志
【发表日期】
：
2021年21期
【关键词】
：
Hemophagocytic lymphohistiocytosis Familial hemophagocytic lymphohistiocytosis P 
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BACKGROUND Familial hemophagocytic lymphohistiocytosis type 2(FHL2)is a rare genetic disorder presenting with fever,hepatosplenomegaly,and pancytopenia secondary to perforin-1(PRF1)mutation.FLH2 has been described in Chinese but usually presents after 1 y
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