Genetic testing helps in identifying changes in chromosomes, genes, or proteins. These tests can confirm or rule out suspected genetic conditions or help determine a person’s chance of developing or passing on a genetic disorder.

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Analyzing an individual’s DNA to identify genetic variations or mutations.

Screening individuals to determine if they carry a gene mutation associated with a genetic disorder, which could be passed on to their offspring.

Assessing the genetic health of a fetus during pregnancy, typically through procedures like amniocentesis or chorionic villus sampling.

Testing newborns for certain genetic conditions shortly after birth to enable early intervention and treatment.

Identifying genetic mutations associated with specific conditions before symptoms manifest, allowing individuals to make informed decisions about their health.


Genetic testing enables the early detection of genetic disorders, facilitating timely intervention and treatment.

By understanding a person’s genetic makeup, healthcare providers can tailor treatment approaches to individual needs, optimizing outcomes.

Knowledge of genetic risks empowers individuals and couples to make informed decisions about family planning, such as whether to undergo prenatal testing or pursue assisted reproductive technologies.

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