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:: دوره 1، شماره 3 - ( 10-1388 ) ::
جلد 1 شماره 3 صفحات 117-115 برگشت به فهرست نسخه ها
A case report of 5 y/o girl with familial chylomicronemia
چکیده:   (7325 مشاهده)
Background: Familial chylomicronemia syndrome is a rare disorder of lipoprotein metabolism due to familial lipoprotein lipase or apolipoprotein C-II deficiency or the presence of inhibitors to lipoprotein lipase. It manifests as eruptive xanthomas, acute pancreatitis, and lipaemic plasma due to marked elevation of triglyceride and chylomicrons levels.
Case presentation: We report a rare case of familial chylomicronemia in a 5 year old girl who was diagnosed after her plasma was incidentally found to be milky. Lipid profile showed familial chylomicronemia. The girl was advised on a low fat diet and a regular follow up check up.
Conclusion: Pediatricians should be alerted for the possibility of familial hyperchylomicronemia due to apolipoprotein CII deficiency and initiate appropriate treatment.
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نوع مطالعه: Original Article | موضوع مقاله: Infectious Diseases
دریافت: 1392/10/24 | پذیرش: 1392/10/24 | انتشار: 1392/10/24
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Eshraghi P, Esmaili Dooki M R, Bakhshandeh Bali M K. A case report of 5 y/o girl with familial chylomicronemia. Caspian J Intern Med. 2010; 1 (3) :115-117
URL: http://caspjim.com/article-1-86-fa.html

A case report of 5 y/o girl with familial chylomicronemia. 1. 1388; 1 (3) :117-115

URL: http://caspjim.com/article-1-86-fa.html



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دوره 1، شماره 3 - ( 10-1388 ) برگشت به فهرست نسخه ها
Caspian Journal of Internal Medicine
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