The symptoms and severity of dermatological diseases are extremely broad and highly variable. Most skin diseases are polygenic, meaning that — many different genes are involved. By identifying disease-causing variants through our comprehensive genetic tests, you can provide your patients with a more precise medical prognosis.
CentoSkin is our diagnostic test for patients displaying skin disorders. Our panel includes genes for hypotricosis, epidermolysis bullosa, and congenital ichthyosis, among others. In addition, CentoSkin tests for albinism and other conditions with similar pigmentation abnormalities such as Hermasky-Pudlak syndrome, Griscelli snydrome and Waardenburg syndrome.
Learn more| TAT | 25 business days |
| Coverage | ≥99.00% ≥20x |
| Methods | NGS including CNV analysis |
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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