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The most complete carrier screening panel

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:

Who should consider CentoScreen®

The CentoScreen® advantage

Comprehensive screening panel of 331 autosomal and X-linked recessive disorders

Sequencing at ≥ 20x coverage

CNV reporting for 34 genes

Additional assays for SMN1, FMR1 & CYP21A2 included

Turnaround time of 15 business days

Patterns of inheritance examined by CentoScreen®

Autosomal recessive disorder

CentoScreen Autosomal disorder inheritance pattern

X-linked recessive disorder

CentoScreen Recessive disorder inheritance pattern
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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

CentoScreen® testing options

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