Subclinical course of cholesterol ester storage disease (CESD) diagnosed in adulthood

Author:

Elleder M.,Ledvinová J.,Cieslar P.,Kuhn R.

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,General Medicine,Pathology and Forensic Medicine,Pathology and Forensic Medicine

Reference29 articles.

1. Assmann G, Fredrickson DS (1983) Acid lipase deficiency: Wolman's disease and cholesteryl ester storage disease. In: Stanbury JB, Wyngaarden JB, Fredrickson DS, Goldstein JL, Brown M (eds) Metabolic basis of inherited diesease. McGraw-Hill, New York, pp 803–819

2. Beaudet AL, Lipson MH, Ferry GD, Nichols BR Jr (1974) Acid lipase in cultured fibroblasts: cholesterol ester storage disease. J Lab Clin Med 84:54–61

3. Besley GTN, Broadhead DM, Laulor E (1984) Acid esterase deficiency: comparison of biochemical findings in infantile and adult forms. J Inher Metab Dis 7, Suppl 2:155–156

4. D'Agostino D, Bay L, Gallo G, Chamoles N (1988) Cholesterol ester storage disease: clinical, biochemical, and pathological studies of four new cases. J Pediatr Gastroenterol Nutr 7:446–450

5. Dincsoy HP, Rolfes DB, McGraw CA, Schubert WK (1984) Cholesterol ester storage disease and mesenteric lipodystrophy. J Clin Pathol 81:263–269

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