Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78-year-old patient

Author:

Jurecka Agnieszka,Stiburkova Blanka,Krijt Jakub,Gradowska Wanda,Tylki-Szymanska Anna

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference10 articles.

1. Arikyants N, Sarkissian A, Hesse A, Eggermann T, Leumann E, Steinmann B (2007) Xanthinuria type I: a rare cause of urolithiasis. Pediatr Nephrol 22:310–314

2. Blake DR, Stevens CR, Sahinoglu T et al (1997) Xanthine oxidase: four roles for the enzyme in rheumatoid pathology. Biochem Soc Trans 25:812–816

3. Bradford MJ, Hrehorovich V (1969) Xanthinuria, psoriasis and arthritis. Am J Med 46:137–141

4. Engelman K, Watts RW, Klinenberg JR, Sjoerdsma A, Seegmiller JE (1966) Clinical physiological exercise and biochemical studies of a patient with xanthinuria and pheochromocytoma. Am J Med 37:836–861

5. Freudweiler M (1901) Experimentelle Untersuchungen uber die Entstchung der Gichtknoten. Deutches Arch Klin Med 69:155

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