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- W2063799609 abstract "IDIOPATHIC familial hyperlipemia is a rare disorder. Hyperlipemia associated with certain known pathologic conditions is not uncommon; it may be found in cases of diabetes mellitus, certain diseases of the kidney, liver and pancreas, hypothyroidism, starvation, anemia, occlusive vascular disease, certain dermatoses, glycogenosis (von Gierke's disease) and Niemann-Pick disease. Only seven cases of idiopathic hyperlipemia in children are found in the literature, 1 with an equal number in adults being reported. 2 Burger and Grutz 1a (1932) described the first case, of an 11 year old boy with hyperlipemia, hepatosplenomegaly and a nodular xanthomatous skin eruption which appeared and disappeared with rise and fall of the blood lipid level. Opitz 1b (1935) described a 12 year old boy with hyperlipemia and splenomegaly but without xanthomatous skin eruption. Franklin 1c (1937) reported a case of a 5 year old girl who had no skin lesions but had splenomegaly and hyperlipemia. Bernstein" @default.
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- W2063799609 date "1951-08-01" @default.
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- W2063799609 title "IDIOPATHIC FAMILIAL HYPERLIPEMIA" @default.
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- W2063799609 doi "https://doi.org/10.1001/archpedi.1951.02040040162006" @default.
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