Infantile familial chylomicronemia syndrome caused by LPL gene variants coexisting with renal hamartoma:A case report
10.3969/j.issn.1001-5256.2023.04.022
- 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
1. The Center for Pediatric Liver Diseases, Children's Hospital of Fudan University, Shanghai 201102, China
2. Department of Gastroenterology, Wuxi Children's Hospital, Wuxi, Jiangsu 214023, China
3. Department of Clinical Nutrition, Children's Hospital of Fudan University, Shanghai 201102, China
- Publication Type:Case Report
- Keywords:
Hyperlipoproteinemia Type I;
Hypertriglyceridemia;
Renal Hamartoma
- From:
Journal of Clinical Hepatology
2023;39(4):896-900
- CountryChina
- Language:Chinese