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[Rotor's syndrome. Apropos of a case].

作者信息

Carre D, Civadier C, Foll Y, Talarmin B, Abgrall J

机构信息

Service de Gastroentérologie, Hôpital d'Instruction des Armées C.-Tonnerre, Brest Naval.

出版信息

Ann Gastroenterol Hepatol (Paris). 1994 Nov-Dec;30(6):255-9.

PMID:7847786
Abstract

Rotor's syndrome is a rare hereditary non hemolytic hyperbilirubinemia. The authors report a new case of a 22-year-old man, with chronic asymptomatic fluctuating jaundice. Liver function tests such as alkaline phosphatase, gammaglutamyl transferase and aminotransferase were normal, the same applying to globulin levels. The diagnosis was confirmed by a typical bromsulphalein clearance test, oral cholecystography, and increased total urinary coproporphyrin as well as coproporphyrin isomer I.

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