An Intro to Homozygous Familial Hypercholesterolemia Familial hypercholesterolemia is some sort of genetic disorder that is caused by a defect of chromosome 19. The disorder can be passed genetically to a child from one or both parents. There are two distinctive types of familial hypercholesterolemia, heterozygous FH and homozygous FH avanafil prezzo . Heterozygous FH takes place when a patient has one abnormal duplicate of the LDL receptor gene, transmitted from one mother or father; homozygous FH occurs when there are two irregular copies of the LDL receptor gene, exceeded from both parents.
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