一名特发性血色素沉着症患者的III型高脂蛋白血症。
Type III hyperlipoproteinemia in a patient with idiopathic hemochromatosis.
作者信息
Feussner G, Ziegler R
机构信息
Abteilung Innere Medizin I, Schwerpunkt Endokrinologie und Stoffwechsel, Heidelberg, Federal Republic of Germany.
出版信息
Hum Genet. 1991 Jan;86(3):326-8.
A 60-year-old man is reported with idiopathic hemochromatosis and type III hyperlipoproteinemia. Regular phlebotomy therapy and fenofibrate treatment favorably influenced the disorder of iron metabolism and the lipid disease. Evidence is given that both errors of metabolism are independently inherited diseases, although the symptoms of the first (idiopathic hemochromatosis) may aggravate the expression of the second (type III hyperlipoproteinemia).
据报道，一名60岁男性患有特发性血色素沉着症和III型高脂蛋白血症。定期放血疗法和非诺贝特治疗对铁代谢紊乱和脂质疾病产生了有利影响。有证据表明，这两种代谢紊乱都是独立的遗传性疾病，尽管第一种疾病（特发性血色素沉着症）的症状可能会加重第二种疾病（III型高脂蛋白血症）的表现。
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