Xanthinuria - An unusual cause for renal stone disease

Journal of Association of Physicians of India

Volumn 44, Issue 3, 1996, Pages 203-204

  Thomas, N ^a   Stephen, D C ^a   Abraham, B ^a   Kekre, N ^a   Seshadri, M S ^a  

^a CHRISTIAN MEDICAL COLLEGE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

XANTHINE DERIVATIVE; XANTHINE OXIDASE;

ARTICLE; CASE REPORT; CHEMISTRY; CHILD; DISORDERS OF PURINE AND PYRIMIDINE METABOLISM; HUMAN; MALE; NEPHROLITHIASIS; URINE;

CHILD; HUMANS; KIDNEY CALCULI; MALE; PURINE-PYRIMIDINE METABOLISM, INBORN ERRORS; XANTHINE OXIDASE; XANTHINES;

EID: 0030089853     PISSN: 00045772     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Smith LH. Endocrinol and Metab Clin North Am 1990; 19 : 4. 767-965.
2. Holmes EW, Wyngaarden JB. Hereditary Xanthinuria. In: Schriver CR, Beaudet AL, Sly WS et al. (Eds) The metabolic basis of inherited disease Vol I, 6th edition, New York, Mcgraw-Hill 1989; 1085-1094.
3. Duran M, Beemer FA, Heiden CVD et al. Combined deficiency of Xanthine oxidase and sulphite oxidase : A defect of molybdenum metabolism or transport. J Inherited metab Dis 1978; 1 : 175-178.
4. Weitz R, Sperling O. Hereditary Renal Hypouricemia. Isolated Tubular defect of urate absorption. J PEDIATR 1980; 96: No. 5, 850-853.
5. T Yamamoto, Y Moriwaki, T Hada et al. An immunoreactive xanthine oxidase protein-possessing xanthinuria and her family. Clinica chimica acta 1992; 208 : 93-98.
6. Kojima T, Nishina T, Kitamura M, Hosoya T, Nishioka K. Biochemical studies on the purine metabolism of four cases with hereditary xanthinuria. Clin Chima Acta 1984; 137 : 189-198.
7. Ichikawa T. Xanthine calculi of kidney. J Urol 1954; 72 : 770-772.