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Familial Hypercholesterolemia is the most common hyperlipoproteinemia during the childhood, which
occurs from the mutation of genes that regulates low-density lipoproteins(LDL), and is classified into
two types, the homozygote presented abnormal genes from both parents and the heterozygote
presented an abnormal gene from each parent. Type IIa familial hypercholesterolemia is characterized
by, especially, increased level of LDL which is common type and normal level... |
