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[Intrahepatic gallstones in patient with alkaptonuria]
Charlotte Bülow1, Jacob Rosenberg
1Herlev Hospital, Kirurgisk afdeling D.
Abstract:
Alkaptonuria is a rare inherited disease with enzyme deficiency in the protein metabolism. The patients accumulate homogentisic acid which leads to symptoms from various body tissues. We describe a patient with recurrent intrahepatic gallstones probably due to such accumulation, and the successful treatment with removal of the stones and a low-protein diet.
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