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Adventia – Genetic Disease Carrier Screening – Fragile X Syndrome

25/03/2025

Fragile X syndrome is an X-linked dominant pathology.

The cause of the disease is a mutation in the FMR1 gene on the X chromosome. This gene ensures the synthesis of the FMRP protein, which plays a crucial role in the formation of neural synapses (connections) and the full mental development of a person.

#Adventia – Fragile X Syndrome Focus Panel, Baseline Panel, and Full Panels – are genetic disease carrier screening tests that examine the carrier status of the gene mutation that causes Fragile X Syndrome.

Adventia – Fragile X Syndrome – Focus Panel

Adventia – full panel (1 person)

Adventia – full panel (2 person)

Adventia – basic panel (1 person)

Adventia – basic panel (2 person)

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