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Hereditary xanthinuria: report on three patients and short review of the literature.
R A RA Frayha, I S IS Salti, A A Arnaout, A A Khatchadurian and S M SM Uthman
Nephron 19(6):328-32 (1977)
PMID 927625
Three patients with hereditary xanthinuria are presented and the pertinent literature is reviewed. In two siblings the disease has been asymptomatic; in the third urolithiasis has developed. Xanthine stone formation is the clinical hallmark of the disease. Hereditary xanthinuria seems to be relatively prevalent in Lebanon.
DOI:
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DOI:
Version: za2963e q8za6 q8zb6 q8zc3 q8zd6 q8zec q8zf9 q8zg8