Two Case Reports of Familial Chylomicronemia Syndrome
Keyword(s):
Type I
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Familial chylomicronemia is a rare autosomal recessive disorder which is also called Hyperlipoproteinemia type I. Here we report two cases with this rare disorder that were admitted to our hospital in recent years.
2019 ◽
Vol 3
(2)
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pp. 84-86
2005 ◽
Vol 129
(5)
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pp. 680-682
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2013 ◽
Vol 88
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pp. 135-137
2016 ◽
Vol 29
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2008 ◽
Vol 11
(1)
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pp. 63-65
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