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These illnesses could be identified by applicable pores and skin checks, tissue studies, serologic examinations, cultures, or specialized staining methods. This syndrome is usually associated with generalized defects in proximal tubule perform similar to Fanconi syndrome, with lack of glycogen, protein, uric acid, and phosphate (Rocher and Tannen, 1986). Nephrolithiasis is unusual in this dysfunction because of comparatively regular urinary citrate excretion (Laing et al. Privacy Policy. Terms & Conditions. Cookies Policy.

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