TITLE

Cystine calculi: challenging group of stones

AUTHOR(S)
Ahmed, Kamran; Dasgupta, Prokar; Khan, Mohammad Shamim
PUB. DATE
December 2006
SOURCE
Postgraduate Medical Journal;Dec2006, Vol. 82 Issue 974, p799
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Cystinuria is an autosomal recessive disorder in renal tubular and intestinal transport of dibasic amino acids, which results in increased urinary excretion of cystine, ornithine, lysine and arginine. It affects 1 in 20 000 people and is caused by a defect in the rBAT gene on chromosome 2. Development of urinary tract cystine calculi is the only clinical manifestation of this disease. Owing to recurrent episodes of stone formation, these patients require a multi-modal approach to management. The role of medical management and minimally invasive surgery was reviewed for the treatment of cystinuria.
ACCESSION #
23717989

 

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