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EFHC2 Gene Mental Retardation X-Linked EFHC2 Related Genetic Test

Original price was: 5,600 د.إ.Current price is: 4,400 د.إ.

-21%

The EFHC2 gene, located on the X chromosome, has been associated with X-linked mental retardation. The gene’s role in cognitive development is still being explored, but mutations in EFHC2 are believed to contribute to various neurological and developmental disorders. Recognizing the importance of early diagnosis and intervention, DNA Labs UAE offers a specialized genetic test focused on identifying mutations in the EFHC2 gene. This test is particularly relevant for families with a history of X-linked mental retardation, providing them with crucial information that can guide management and treatment options.

The test is conducted using a sample of the patient’s DNA, typically extracted from a blood sample. Advanced molecular techniques are employed to meticulously analyze the EFHC2 gene for any abnormalities that might indicate a predisposition to mental retardation and other related conditions. This targeted approach allows for a high degree of specificity and accuracy in diagnosing conditions related to the EFHC2 gene.

Priced at 4400 AED, the EFHC2 related genetic test at DNA Labs UAE is an investment in understanding and potentially mitigating the impact of X-linked mental retardation in affected individuals and their families. The cost reflects the sophisticated technology and expertise required to conduct such specialized genetic testing. For families dealing with the challenges of X-linked mental retardation, this test offers a pathway to gaining valuable insights into their condition, enabling informed decisions about care and support.

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  • This test is not intended for medical diagnosis or treatment
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EFHC2 Gene Mental Retardation X-Linked EFHC2 Related Genetic Test

Test Name: EFHC2 Gene Mental retardation x-linked EFHC2 related 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 EFHC2 Gene Mental retardation, x-linked, EFHC2 related NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with EFHC2 Gene Mental retardation, x-linked, EFHC2 related.

Test Details

Mental retardation, X-linked, EFHC2 related NGS genetic test is a type of genetic test that is used to identify mutations in the EFHC2 gene that are associated with X-linked mental retardation. X-linked mental retardation refers to intellectual disability that is inherited through the X chromosome.

NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the rapid and efficient sequencing of large amounts of DNA. In the context of this genetic test, NGS is used to analyze the EFHC2 gene and identify any mutations or variations that may be present.

The EFHC2 gene is involved in the development and functioning of the brain. Mutations in this gene have been found to cause X-linked mental retardation, which is characterized by intellectual disability, delayed development, and other neurological symptoms.

By performing this genetic test, healthcare professionals can identify individuals who have mutations in the EFHC2 gene and provide them with appropriate medical care and support. It can also help in genetic counseling and family planning by providing information about the risk of passing on the condition to future generations.

Test Name EFHC2 Gene Mental retardation x-linked EFHC2 related 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 EFHC2 Gene Mental retardation, x-linked, EFHC2 related NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with EFHC2 Gene Mental retardation, x-linked, EFHC2 related
Test Details

Mental retardation, X-linked, EFHC2 related NGS genetic test is a type of genetic test that is used to identify mutations in the EFHC2 gene that are associated with X-linked mental retardation. X-linked mental retardation refers to intellectual disability that is inherited through the X chromosome.

NGS (Next-Generation Sequencing) is a high-throughput DNA sequencing technology that allows for the rapid and efficient sequencing of large amounts of DNA. In the context of this genetic test, NGS is used to analyze the EFHC2 gene and identify any mutations or variations that may be present.

The EFHC2 gene is involved in the development and functioning of the brain. Mutations in this gene have been found to cause X-linked mental retardation, which is characterized by intellectual disability, delayed development, and other neurological symptoms.

By performing this genetic test, healthcare professionals can identify individuals who have mutations in the EFHC2 gene and provide them with appropriate medical care and support. It can also help in genetic counseling and family planning by providing information about the risk of passing on the condition to future generations.