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A Case of Lipoprotein Lipase Deficiency inan Infant with Recurrent Pancreatitis / 대한소아소화기영양학회지
Article in Ko | WPRIM | ID: wpr-25026
Responsible library: WPRO
ABSTRACT
Familial chylomicronemia syndrome is a rare disorder characterized by severe hypertriglyceridemia and fasting chylomicronemia. Causes of the syndrome include lipoprotein lipase (LPL) deficiency, apolipoprotein C-II deficiency, or the presence of inhibitors to LPL. We managed a 3-month-old girl who had recurrent acute pancreatitis caused by chylomicronemia. We report the first case of familial chylomicronemia in Korea caused by LPL deficiency in an infant with recurrent acute pancreatitis.
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Full text: 1 Index: WPRIM Main subject: Pancreatitis / Hypertriglyceridemia / Fasting / Korea / Lipoprotein Lipase / Hyperlipoproteinemia Type I / Lipoproteins Limits: Humans / Infant Country/Region as subject: Asia Language: Ko Journal: Korean Journal of Pediatric Gastroenterology and Nutrition Year: 2009 Type: Article
Full text: 1 Index: WPRIM Main subject: Pancreatitis / Hypertriglyceridemia / Fasting / Korea / Lipoprotein Lipase / Hyperlipoproteinemia Type I / Lipoproteins Limits: Humans / Infant Country/Region as subject: Asia Language: Ko Journal: Korean Journal of Pediatric Gastroenterology and Nutrition Year: 2009 Type: Article