Type III hyperlipoproteinemia in a patient with idiopathic hemochromatosis
β Scribed by G. Feussner; R. Ziegler
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 251 KB
- Volume
- 86
- Category
- Article
- ISSN
- 0340-6717
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β¦ Synopsis
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).
π SIMILAR VOLUMES
We report on a 20-year-old man with the combination of two independent familial lipoprotein disorders: heterozygous familial hypercholesterolemia (FH) and type I11 hyperlipoproteinemia (HLP). Familial hypercholesterolemia was diagnosed by elevated total and low density lipoprotein cholesterol levels