Advances in genetic techniques now enable many important insights into kidney-related diseases. A genetic diagnosis can better classify disease, give information about disease pathogenesis, and suggest time-sensitive options for treatment. We have identified genetic variants associated with nephrological diseases in more than 300 different genes. We can support you in providing your patients with rapid and accurate genetic testing to give them a clear understanding of their condition.
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 the most prevalent hereditary kidney disorders, including: alport syndrome, renal tubular acidosis panel, focal glomerulonephrosis panel, and primary hyperoxaluria, among others. CentoNephro also covers the group of disorders causing cilia dysfunction, including Joubert Syndrome, Bardet-Biedl, COACH syndrome, primary ciliary dyskinesia, Meckel syndrome, skeletal dysplasia, situs inversus, and heterotaxy, among others.
Learn more| TAT | 25 business days |
| Coverage | ≥99.00% ≥20x |
| Methods | NGS including CNV analysis |
If polycystic kidney disease is suspected CentoNephro Plus is recommended, which includes all genes of CentoNephro and PKD1 analysis.
Learn more| TAT | 25 business days |
| Coverage | ≥99.00% ≥20x |
| Methods | Sanger sequencing |
Whole Genome Sequencing (WGS), offers the most comprehensive one-step solution with the highest diagnostic yield
Whole Exome Sequencing (WES) enables quicker and cost-effective diagnosis for patients with complex and unclear symptoms
Multiomics give a deeper understanding of human biological processes and acts as a unique and highly effective tool for early diagnosis
Create a diagnostic gene panel by selecting genes tailored to individual patient needs.
2 to >4.000
Selectable Genes
15 Business Days
TAT
Genome or Exome
Backbone
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