The ear is essential for many of our most basic functions. It is crucial to distinguish between genetic disorders and those caused by environmental factors as early as possible. Rapid and informative postnatal testing for genetic disorders of the ear, nose, and throat allow for genetic counseling and may facilitate early interventions to significantly improve prognoses. We have identified genetic variants associated with diseases related to hearing -loss in over 190 different genes. Our testing options can help pinpoint the exact cause of inherited deafness and related syndromes.
Hearing loss is a common condition in children, affecting 1 in 100 live births. In more than 50% of the cases, there is a genetic cause for this disorder, from which 70% cause non-syndromic hearing loss. CentoHear includes genes associated with syndromic and non-syndromic hearing loss. Both autosomal recessive and dominant cases are included in the panel. In addition, CentoHear includes syndromes, such as Alport, Pendred, Waardenburg, Usher, and branchio-oto-renal among others.
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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