The earliest step to responsible family planning

CentoScreen® is the most complete carrier screening panel helping healthy couples understand if they are carriers of up to 331 relevant recessive genetic diseases before pregnancy.

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:

Who should consider CentoScreen®

The CentoScreen® advantage

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

Full gene sequencing at ≥ 20x coverage

CNV reporting for 34 genes

Additional assays for SMN1, FMR1 & CYP21A2 included

Turnaround time of 14 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

Ready to get started ?

Order your test

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