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FGD1 Gene Mental Retardation X-Linked Type 16 Genetic Test

4,400 د.إ

-21%

The FGD1 Gene Mental Retardation X-Linked Type 16 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the FGD1 gene, which are associated with X-linked mental retardation type 16 (MRX16). This condition is a rare genetic disorder that affects cognitive function and can lead to various degrees of intellectual disability. The test aims to provide crucial information for the accurate diagnosis and management of individuals suspected to have MRX16, enabling targeted interventions and support.

Carried out through advanced genetic sequencing techniques, the test analyzes the FGD1 gene for specific mutations that are known to cause the disorder. This is particularly important for families with a history of the condition, as it can help in understanding the risk for future generations.

The cost of the FGD1 Gene Mental Retardation X-Linked Type 16 Genetic Test at DNA Labs UAE is 4400 AED. The investment in this test can be invaluable for affected families, offering them insights into the genetic underpinnings of the condition and guiding them towards appropriate medical and psychological support services. It’s a critical step in the journey towards personalized medicine, where treatments and interventions can be tailored to the individual based on their unique genetic makeup.

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FGD1 Gene Mental Retardation X-linked Type 16 Genetic Test

Test Name: FGD1 Gene Mental retardation X-linked type 16 Genetic Test
Components: Blood or Extracted DNA or One drop Blood on FTA Card
Price: 4400.0 AED
Sample Condition: Blood or Extracted DNA or One drop Blood on FTA Card
Report Delivery: 3 to 4 Weeks
Method: NGS Technology
Test Type: Neurological Disorders
Doctor: Neurologist
Test Department: Genetics
Pre Test Information: Clinical History of Patient who is going for FGD1 Gene Mental retardation, X-linked type 16 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with FGD1 Gene Mental retardation, X-linked type 16
Test Details: FGD1 gene, also known as Faciogenital Dysplasia 1 gene, is a gene located on the X chromosome. Mutations in this gene are associated with a condition called Mental Retardation, X-linked type 16 (MRX16). NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of various genetic variations, including single nucleotide variants, insertions, deletions, and structural variations. In the case of MRX16, an NGS Genetic Test can be used to analyze the FGD1 gene for any pathogenic mutations or variations. This test can help diagnose individuals with MRX16 and provide information about the genetic cause of their condition. By identifying the specific genetic variant in the FGD1 gene, NGS Genetic Test can also assist in genetic counseling and family planning decisions. It can help determine the likelihood of passing on the condition to future generations and provide information about potential treatment options or management strategies. It is important to note that genetic testing, including NGS Genetic Test, should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the test results.

Test Name FGD1 Gene Mental retardation X-linked type 16 Genetic Test
Components
Price 4400.0 AED
Sample Condition Blood or Extracted DNA or One drop Blood on FTA Card o
Report Delivery 3 to 4 Weeks
Method NGS Technology
Test type Neurological Disorders
Doctor Neurologist
Test Department: Genetics
Pre Test Information Clinical History of Patient who is going for FGD1 Gene Mental retardation, X-linked type 16 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with FGD1 Gene Mental retardation, X-linked type 16
Test Details

FGD1 gene, also known as Faciogenital Dysplasia 1 gene, is a gene located on the X chromosome. Mutations in this gene are associated with a condition called Mental Retardation, X-linked type 16 (MRX16).

NGS (Next-Generation Sequencing) Genetic Test is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for the detection of various genetic variations, including single nucleotide variants, insertions, deletions, and structural variations.

In the case of MRX16, an NGS Genetic Test can be used to analyze the FGD1 gene for any pathogenic mutations or variations. This test can help diagnose individuals with MRX16 and provide information about the genetic cause of their condition.

By identifying the specific genetic variant in the FGD1 gene, NGS Genetic Test can also assist in genetic counseling and family planning decisions. It can help determine the likelihood of passing on the condition to future generations and provide information about potential treatment options or management strategies.

It is important to note that genetic testing, including NGS Genetic Test, should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support based on the test results.