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      Severe chronic diarrhea and weight loss in cholesteryl ester storage disease: a case report.

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          Abstract

          An inherited deficiency of human lysosomal acid lipase (LAL) results in the rare conditions of Wolman disease and cholesteryl ester storage disease (CESD). We want to present the rare case of CESD in an adult.

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          Author and article information

          Journal
          World J. Gastroenterol.
          World journal of gastroenterology
          1007-9327
          1007-9327
          Apr 21 2005
          : 11
          : 15
          Affiliations
          [1 ] Institute of Pathology, University of Cologne, Joseph-Stelzmann-Strasse 9, D-59031 Cologne, Germany. u.drebber@uni-koeln.de
          Article
          4305829
          15818756
          4f4dba38-2b77-4fd3-aae3-e641591617dd
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