HERC2 Gene Mental Retardation Autosomal Recessive Type 38 Genetic Test
At DNA Labs UAE, we offer the HERC2 Gene Mental Retardation Autosomal Recessive Type 38 Genetic Test at a cost of AED 4400.0.
Test Details
The HERC2 gene is associated with a condition called mental retardation, autosomal recessive type 38 (MRT38). Individuals with this condition experience intellectual disability, developmental delay, and other neurological abnormalities.
Our Genetic Test utilizes NGS (Next-Generation Sequencing) technology to analyze multiple genes simultaneously. Specifically, it focuses on identifying mutations or variations in the HERC2 gene that may be responsible for the condition. By analyzing this gene, our test can provide valuable information about the specific genetic changes contributing to the individual’s symptoms.
Obtaining a definitive diagnosis through this genetic test can help in understanding the underlying cause of the condition and potentially guide treatment options or management strategies.
Test Components and Price
- Test Name: HERC2 Gene Mental Retardation Autosomal Recessive Type 38 Genetic Test
- Price: AED 4400.0
Sample Condition
We accept the following sample conditions:
- Blood
- Extracted DNA
- One drop of blood on FTA Card
Report Delivery
Reports are typically delivered within 3 to 4 weeks.
Test Method
Our Genetic Test utilizes NGS (Next-Generation Sequencing) technology.
Test Type
This test focuses on Neurological Disorders.
Referring Doctor
Our Neurologist will oversee the testing process.
Test Department
Our Genetics department handles the HERC2 Gene Mental Retardation Autosomal Recessive Type 38 Genetic Test.
Pre Test Information
Prior to the test, we require the following:
- Clinical History of the Patient who is going for HERC2 Gene Mental Retardation Autosomal Recessive Type 38 NGS Genetic DNA Test
- A Genetic Counselling session to draw a pedigree chart of family members affected with HERC2 Gene Mental Retardation Autosomal Recessive Type 38
It is important to consult with a healthcare professional or genetic counselor to discuss the specific implications and limitations of the HERC2 gene testing in the context of mental retardation, autosomal recessive type 38. They can provide personalized guidance and support based on the individual’s specific situation and family history.
Test Name | HERC2 Gene Mental retardation autosomal recessive type 38 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 HERC2 Gene Mental retardation, autosomal recessive type 38 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HERC2 Gene Mental retardation, autosomal recessive type 38 |
Test Details |
The HERC2 gene is associated with a condition called mental retardation, autosomal recessive type 38 (MRT38). This condition is characterized by intellectual disability, developmental delay, and other neurological abnormalities. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to analyze multiple genes simultaneously. In the context of MRT38, NGS genetic testing can be used to identify mutations or variations in the HERC2 gene that may be responsible for the condition. By analyzing the HERC2 gene, NGS genetic testing can provide valuable information about the specific genetic changes that may be contributing to the individual’s symptoms. This can help in making a definitive diagnosis, understanding the underlying cause of the condition, and potentially guiding treatment options or management strategies. It is important to consult with a healthcare professional or a genetic counselor to discuss the specific implications and limitations of the HERC2 gene testing in the context of mental retardation, autosomal recessive type 38. They can provide personalized guidance and support based on the individual’s specific situation and family history. |