'Cystine' presentation slideshows

CYSTINURIA

CYSTINURIA. By DR Jameel Tariq Miro. Cystinuria is an autosomal recessive defect in reabsorptive transport of cystine and the dibasic amino acids ornithine, arginine, and lysine from the luminal fluid of the renal proximal tubule and small intestine. Pathophysiology.

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Definitions

Nephropathic cystinosis: 10 th anniversary of the CTNS gene Elena Levtchenko, MD, PhD University Hospital Leuven, Belgium. Definitions. Cystinosis an autosomal recessive disease caused by lysosomal accumulation of cystine due to defective exodus of cystine out of the lysosomes Cystinosis

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Microcrystal in human urine

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