Congenital steatosis of the liver: biochemical approach to its pathogenesis.

نویسندگان

  • K TADA
  • N KATSUSHIMA
  • H HIRONO
  • T ARAKAWA
چکیده

glycemia and a poor response of blood sugar to the adrenaline test. From veiw point of clinical features congenital steatosis of the liver is unable to be dif ferentiated from glycogen storage disease of the liver.1,2) The differential diagnosis between them is achieved only by liver biopsy•\conspicuous fatty liver in congenital steatosis, which is not a common finding of the liver in glycogen storage disease.1, 2) It is, however, not seldom to find the descriptions of accumulation of both glycogen and fat in hepatic cells among the reported cases of glycogen storage disease with liver biopsy.3) In 1934, Debre et al .4) advocated a new conception: "hepatomegalie

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عنوان ژورنال:
  • The Tohoku journal of experimental medicine

دوره 77  شماره 

صفحات  -

تاریخ انتشار 1962