Nephron. 1977;19(6):328-32.

Hereditary xanthinuria: report on three patients and short review of the literature.

Frayha RA, Salti IS, Arnaout A, Khatchadurian A, Uthman SM.

Abstract

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.

PMID:: 927625; [PubMed - indexed for MEDLINE]

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Xanthines

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[Three cases of hereditary xanthinuria: review of the literature (author's transl)]. [Sem Hop. 1979]
[Three cases of hereditary xanthinuria: review of the literature (author's transl)].
Temperville B, Godin M, Dubois D, Fillastre JP. Sem Hop. 1979 Dec 8-15; 55(41-42):1899-902.
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Cartier P, Perignon JL. Nouv Presse Med. 1978 Apr 22; 7(16):1381-90.
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Hereditary xanthinuria: report on three patients and short review of the literature.

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