Neurological Abnormality Could be the First and Only Symptom of Familial Hemophagocytic Lymphohistiocytosis: Report of Two Families.
- Author:
Yun-Ze ZHAO
1
,
2
,
3
,
4
;
Hua CHENG
5
;
Chang-Hong DING
6
;
Hong-Hao MA
1
,
2
,
3
,
4
;
Tong-Li HAN
6
;
Jiu-Wei LI
6
;
Dong WANG
1
,
2
,
3
,
4
;
Zhi-Gang LI
1
,
2
,
3
,
4
;
Tian-You WANG
1
,
2
,
3
,
4
;
Rui ZHANG
1
,
2
,
3
,
4
Author Information
- Publication Type:Case Reports
- MeSH: Central Nervous System Diseases; etiology; Child; Female; Humans; Infant; Lymphohistiocytosis, Hemophagocytic; complications; diagnosis; genetics; Magnetic Resonance Imaging; Male; Mutation; Perforin; genetics
- From: Chinese Medical Journal 2018;131(24):3004-3006
- CountryChina
- Language:English