Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Cystinuria

This disease is characterized by kidney stone fomation due to increased renal excretion of the amino acid cystein. The stones are made of cystine.

Epidemiology

The Cystinurie is one of the most frequent hereditary diseases.The frequency is indicated in our population as 1:7000.

Test Strategy

The Cystinuria can be mesured in quantitatively. Kidney stones should be investigated. If there something indicates for cystinuria a genetic test can be performed.

Pathogenesis

The filtered amino acid could not be reabsorbed adequately because of a defect in the transporter of dibasic amino acids.

Systematic

Urolithiasis
Cystinuria
SLC3A1
SLC7A9
Dicarboxylic aminoaciduria
Dihydroxyadenin urolithiasis
Nephrocalcinosis
Nephrolithiasis diarrhea syndrome
Susceptibility to nephrolithiasis
Uric acid nephropathy
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