A Case of Lipoprotein Lipase Deficiency inan Infant with Recurrent Pancreatitis / 대한소아소화기영양학회지
Korean Journal of Pediatric Gastroenterology and Nutrition
; : 79-83, 2009.
Article
ي Ko
| WPRIM
| ID: wpr-25026
المكتبة المسؤولة:
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.
Key words
النص الكامل:
1
الفهرس:
WPRIM
الموضوع الرئيسي:
Pancreatitis
/
Hypertriglyceridemia
/
Fasting
/
Korea
/
Lipoprotein Lipase
/
Hyperlipoproteinemia Type I
/
Lipoproteins
المحددات:
Humans
/
Infant
البلد/الأقليم حسب الموضوع:
Asia
اللغة:
Ko
مجلة:
Korean Journal of Pediatric Gastroenterology and Nutrition
السنة:
2009
نوع:
Article