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What does CSNU stand for?

CSNU stands for Cystinuria

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Samples in periodicals archive:

Dr Moussa said the primary known causes are inadequate urinary drainage; dehydration and lack of sufficient fluid ingestion; foreign bodies in the urinary tract; diet with excess oxalates, calcium, and vitamin abnormalities such as vitamin A deficiencies, vitamin D excess; urinary infections; metabolic diseases (hyper-parathyroidism, cystinuria, gout, intestinal dysfunction); and use of certain medications such as diuretics, that increase the levels of uric acid.
To the Editor: Cystinuria is an inherited form of nephrolithiasis caused by mutations in the SLC7A9 [1] [solute carrier family 7 (cationic amino acid transporter, y+ system), member 9] and SLC3A1 [solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1] genes, which encode the luminal transporter b(0, +) AT subunit and rBAT subunit, respectively.
org 1,2,3,4,5,7 videos and cassettes available HYDROCEPHALUS, OBSTRUCTIVE See: Dandy-Walker Syndrome HYPERAMMONEMIA See: Urea Cycle Disorders HYPERBILIRUBINEMIA See: Kernicterus HYPERCALCEMIA SYNDROME, INFANTILE, IDIOPATHIC See: Williams Syndrome HYPERCALCEMIA-SUPRAVALVAR AORTIC STENOSIS See: Williams Syndrome HYPERCYSTINURIA See: Cystinuria HYPERGLYCINEMIA WITH KETOACIDOSIS AND LEUKOPENIA See: Acidemia, Organic HYPERLEXIA See: Autism Canadian Hyperlexia Association 300 John St.
Several genetic defects in specific carriers needed for tubular reabsorption of specific amino acids cause aminoaciduria, including cystinuria and Hartuup disease.