CENTOGENE provides genetic testing and consultation for the most efficient diagnosis of inherited kidney-related diseases. Recent advances in genetic techniques provide many important insights into kidney disease diagnosis, classification, pathogenesis, and time-sensitive therapy options. Having identified genetic variants associated with nephrological diseases in more than 300 different genes, we can support you in providing your patients with rapid, effective genetic testing to get a clear understanding of their condition.
Atypical hemolytic uremic syndrome panel
Our atypical hemolytic uremic syndrome panel contains genes for the molecular diagnosis of atypical hemolytic uremic syndrome.
|No. of genes:||20|
|Details:||MLPA: CFH, CFHR1, CFHR2, CFHR3, CFHR5|
COMMON SYNDROMES AND DISORDERS COVERED
Atypical Hemolytic Uremic syndrome
Approximately 10% of the population worldwide is affected by chronic kidney diseases. Advances in genetic techniques are providing insights into kidney disease diagnosis, pathogenesis, and therapy. CentoNephro offers a comprehensive tool to screen for most prominent hereditary kidney disorders, including polycystic kidney disease, Alport syndrome, renal tubular acidosis panel, focal glomerulonephrosis panel, and primary hyperoxaluria, among others. PDK1 analysis is not included in this panel.
|No. of genes:||303|
If polycystic kidney disease is suspected CentoNephro Plus is recommended, which includes PKD1 analysis.
|No. of genes:||304|
|Details:||with CNV and PKD1 analysis|