Help your patients make an informed decision
Most people can be carriers of a disease causing change without knowing it. If both partners are carriers, they have a 25% risk of having an affected child with a recessive genetic disease and a 50% that the child will be a carrier like the parents.
CentoScreen® is appropriate for individuals or couples with the following backgrounds, and can be offered before or in early pregnancy:
The CentoScreen® advantage
Autosomal recessive disorder
X-linked recessive disorder
Why choose CentoScreen®?
CentoScreen® is the most complete genetic screening test with ≥99% coverage of 331 genes, providing couples and physicians with the highest confidence in test results.
The 331 disorders were selected based on the following criteria:
1. High carrier frequency
2. Well-defined phenotype
3. Early onset of disease
4. Highly severe phenotype
5. Affected quality of life
6. Availability of surgical and medical treatment
CentoScreen® testing options
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