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Information Journal Paper

Title

A CASE REPORT OF CAROLI SYNDROME

Author(s)

GHANA SAMIEH | SANAGOO AKRAM | JOUYBARI LEILA (MAHASTI) | Issue Writer Certificate 

Pages

  143-147

Abstract

 Background: Caroli disease is a rare inherited disorder characterized by dilatation of the intrahepatic bile ducts.Case report: The presented case is a female middle age patient that during clinical and para-clinical evaluation for an unrelated compliant found that has Caroli disease. Although, the disease is hereditary but the family history was negative. After three years follow up, no involvement of kidney or serious damage of live is reported.Conclusion: Prognosis is fairly good unless recurrent cholangitis and renal failure develops. Since the disease has slow and silent progress while is rare and fatal, it should be considered as differential diagnosis in any unknown cholangitis case.

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  • Cite

    APA: Copy

    GHANA, SAMIEH, SANAGOO, AKRAM, & JOUYBARI, LEILA (MAHASTI). (2011). A CASE REPORT OF CAROLI SYNDROME. JENTASHAPIR JOURNAL OF CELLULAR AND MOLECULAR BIOLOGY (JENTASHAPIR JOURNAL OF HEALTH RESEARCH), 2(3 (4)), 143-147. SID. https://sid.ir/paper/205698/en

    Vancouver: Copy

    GHANA SAMIEH, SANAGOO AKRAM, JOUYBARI LEILA (MAHASTI). A CASE REPORT OF CAROLI SYNDROME. JENTASHAPIR JOURNAL OF CELLULAR AND MOLECULAR BIOLOGY (JENTASHAPIR JOURNAL OF HEALTH RESEARCH)[Internet]. 2011;2(3 (4)):143-147. Available from: https://sid.ir/paper/205698/en

    IEEE: Copy

    SAMIEH GHANA, AKRAM SANAGOO, and LEILA (MAHASTI) JOUYBARI, “A CASE REPORT OF CAROLI SYNDROME,” JENTASHAPIR JOURNAL OF CELLULAR AND MOLECULAR BIOLOGY (JENTASHAPIR JOURNAL OF HEALTH RESEARCH), vol. 2, no. 3 (4), pp. 143–147, 2011, [Online]. Available: https://sid.ir/paper/205698/en

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