Infantile familial chylomicronemia syndrome caused by LPL gene variants coexisting with renal hamartoma:A case report
- VernacularTitle:LPL基因变异导致的婴儿家族性高乳糜微粒血症合并肾脏错构瘤1例报告
- Author:
Xintao CHEN
1
,
2
;
Weiyuan FANG
1
;
Xiaoyan GONG
3
;
Qiong LIN
2
;
Yi LU
1
Author Information
- Publication Type:Case Report
- Keywords: Hyperlipoproteinemia Type I; Hypertriglyceridemia; Renal Hamartoma
- From: Journal of Clinical Hepatology 2023;39(4):896-900
- CountryChina
- Language:Chinese