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Dihydroxyadenine stone with adenine phosphoribosyltransferase deficiency: A case report
Pramod Krishnappa1, Venkatesh Krishnamoorthy1, Kiran Krishne Gowda2
1Department of Urology, NU Hospitals, Bengaluru, Karnataka, India.
Abstract:
Adenine phosphoribosyltransferase (APRT) deficiency is a rare autosomal recessive error of purine metabolism resulting in the generation of 2,8-dihydroxyadenine (DHA), a highly insoluble metabolite of adenine, which can cause radiolucent urolithiasis. This is the second case of DHA stone being reported in India and the first case in India to document the mutation of the APRT gene on blood DNA analysis.
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