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Information Journal Paper

Title

NEONATAL GIANT CELL HEPATITIS IN AN INFANT WITH CYSTIC FIBROSIS

Pages

  193-195

Abstract

 Background: CYSTIC FIBROSIS is a hereditary disease of mucus and sweat glands characterized by respiratory infections and pancreatic insufficiency.Case presentation: We describe a girl infant with CHOLESTASIS as of the first clinical presentation at the age of 1 month. She developed severe anemia which required transfusion for several times. High level of direct bilirubin, low level of albumin and positive sweat tests were detected in laboratory tests. Histopathology report of liver biopsy indicated giant cell NEONATAL HEPATITIS.Conclusion: Although NEONATAL HEPATITIS is common cause of neonatal CHOLESTASIS, such condition is quite rare in CYSTIC FIBROSIS, which easily could be misdiagnosed. Early diagnosis and appropriate treatment could prevent further complications of the disease.

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    APA: Copy

    FALAHI, GHOLAM HOSSEIN, BAZVAND, F., EFTEKHARI, K., AHMADI, FAEZEH, AHMADI, MAEDEH, & REZAEI, NIMA. (2009). NEONATAL GIANT CELL HEPATITIS IN AN INFANT WITH CYSTIC FIBROSIS. IRANIAN JOURNAL OF PEDIATRICS, 19(2), 193-195. SID. https://sid.ir/paper/562534/en

    Vancouver: Copy

    FALAHI GHOLAM HOSSEIN, BAZVAND F., EFTEKHARI K., AHMADI FAEZEH, AHMADI MAEDEH, REZAEI NIMA. NEONATAL GIANT CELL HEPATITIS IN AN INFANT WITH CYSTIC FIBROSIS. IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2009;19(2):193-195. Available from: https://sid.ir/paper/562534/en

    IEEE: Copy

    GHOLAM HOSSEIN FALAHI, F. BAZVAND, K. EFTEKHARI, FAEZEH AHMADI, MAEDEH AHMADI, and NIMA REZAEI, “NEONATAL GIANT CELL HEPATITIS IN AN INFANT WITH CYSTIC FIBROSIS,” IRANIAN JOURNAL OF PEDIATRICS, vol. 19, no. 2, pp. 193–195, 2009, [Online]. Available: https://sid.ir/paper/562534/en

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