β-Sitosterolemia and Xanthomatosis
- 26 February 1976
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 294 (9) , 482-483
- https://doi.org/10.1056/nejm197602262940907
Abstract
Recently, Bhattacharyya and Connor described in two sisters a lipid-storage disease, β-sitosterolemia and xanthomatosis,1 with tendon and tuberous xanthomas appearing at an early age despite normal plasma cholesterol levels. High concentrations of plant sterols, especially β-sitosterol and campesterol, were found in the plasma, red blood cells, xanthomas, adipose tissue and skin. In the following case the same disorder occurred in a patient unrelated to the two sisters originally identified.Case ReportA 31-year-old woman was referred to the National Institutes of Health Lipid Clinic five years ago because of xanthomatosis and mild hypercholesterolemia. Xanthomas, which first appeared at the age . . .This publication has 6 references indexed in Scilit:
- β-Sitosterolemia and XanthomatosisJournal of Clinical Investigation, 1974
- Metabolism of β-sitosterol in manJournal of Clinical Investigation, 1970
- Absorbability of β-sitosterol in humansMetabolism, 1969
- Fat Transport in Lipoproteins — An Integrated Approach to Mechanisms and DisordersNew England Journal of Medicine, 1967
- Fat Transport in Lipoproteins — An Integrated Approach to Mechanisms and DisordersNew England Journal of Medicine, 1967
- Fat Transport in Lipoproteins — An Integrated Approach to Mechanisms and DisordersNew England Journal of Medicine, 1967