Chylomicron retention disease: Difference between revisions

Latest revision as of 13:50, 21 November 2016

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-__NOTOC__
+#REDIRECT[[Hypobetalipoproteinemia]]
-{{SI}}
-{{CMG}}; {{AE}} {{Rim}}
-{{SK}} Anderson disease, lipid transport defect of intestine, hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells
-==Overview==
-Chylomicron retention disease is an autosomal recessive hypolipoproteinemia disease.  Chylomicron retention disease is a very rare condition that is caused by a mutation in SAR1B                                            gene located on chromosome 5q31.1 leading to deficiency in the secretion of apolipoprotein B from enterocytes. While the synthesis chylomicron synthesis is totally affected, VLDL synthesis is intact.
-==References==
-{{Reflist|2}}
-{{lipopedia}}
-[[Category:Lipopedia]]