WES | Premarital Screening Genetic Test

WES examines a wider panel of genes that are responsible for the most complex health conditions.
WES reaches the end of the line for diagnostic options, with no other tests that could be offered.
Classifies information obtained from DNA that has over 24,000 genes.
Advanced NGS (Next Generation Sequencing) technology is used to determine the information obtained from
Results are obtained in 8-9 weeks
More than 20 years of experience

This test is suitable in case of:

For any couple who wants to know the risk of transmitting hereditary genetic disorders to their children.
Before an assisted reproductive treatment (ART) to understand the mutations in the DNA that can lead to affected child.
For couples who have already undergone some genetic testing and is looking for the most extensive genetic tests..
WES may find a genetic cause for your or your child’s signs and symptoms even if previous genetic testing did not.
Individuals with genetic disorders known to have multiple associated genes, or multiple number of clinical signs and symptoms.

Numerous mutations or changes in the DNA that can result in an affected child in the patient’s family.
The main indication of exome sequencing is to characterize an unmapped monogenic genetic disease present in a descendant, recognized as an index patient.
The WES test aims to identify a mutation that explains the symptoms associated with a typically hereditary disease.

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