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Lahalak Medical PlatformDifferentiate Care
Fragile X Syndrome Test
Precise genetic analysis to detect mutations causing Fragile X Syndrome, providing clear insights to support cognitive development and healthy growth for children and families.
The Fragile X Syndrome test is a genetic test used to detect mutations in the FMR1 gene, which is responsible for Fragile X Syndrome, one of the most common genetic causes of intellectual disability. This test is important in diagnosing the syndrome, as symptoms may appear in childhood, such as speech delays, social communication difficulties, and repetitive behaviors. The test is performed by taking a blood sample and analyzing the DNA to determine if there is an increased number of repeats in the FMR1 gene, indicating a risk of developing the syndrome. This test also helps provide essential information for families to understand the genetic risks associated with the syndrome.
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