Abstract
Familial type III hyperlipoproteinemia (synonyms: “floating beta” disorder, familial “broad beta” disease, dysbetalipoproteinemia) is an uncommon genetically determined disorder of lipoprotein metabolism (Fredrickson et al., 1967; Quartfordt et al., 1971; Hazzard et al., 1972; Fredrickson and Levy, 1972). The exact metabolic defect and genetic mode of inheritance are not yet established. It is characterized by an apparent abnormal lipoprotein form, elevation in plasma cholesterol and triglyceride levels, typical cutaneous and subcutaneous lesions and premature peripheral and coronary vessel disease.
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Levy, R.I., Assmann, G. (1976). Type III-Hyperlipoproteinemia. In: Assmann, G., et al. Fettstoffwechsel. Handbuch der inneren Medizin, vol 7 / 4. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-66302-4_10
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DOI: https://doi.org/10.1007/978-3-642-66302-4_10
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