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HSD17B10 Gene Mental Retardation X-Linked Type 17 Genetic Test

4,400 د.إ

-21%

The HSD17B10 gene is associated with a rare condition known as Mental Retardation, X-Linked, Type 17. This genetic disorder is characterized by a spectrum of neurological and developmental issues, including cognitive impairment, speech delays, and, in some cases, behavioral problems. The condition is caused by mutations in the HSD17B10 gene, which is located on the X chromosome, and thus primarily affects males.

To diagnose this condition, a specific genetic test can be performed, which involves analyzing the DNA to identify mutations in the HSD17B10 gene. This test is crucial for confirming the diagnosis, understanding the severity of the condition, and guiding treatment and management decisions.

In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the test is 4400 AED. DNA Labs UAE is equipped with advanced genetic testing facilities to provide accurate and reliable results. Opting for this test at DNA Labs UAE can be a vital step for families seeking answers about the condition and how to best support their loved ones affected by Mental Retardation, X-Linked, Type 17.

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HSD17B10 Gene Mental Retardation X-linked Type 17 Genetic Test

At DNA Labs UAE, we offer the HSD17B10 Gene Mental Retardation X-linked Type 17 Genetic Test. This test is designed to diagnose mental retardation, X-linked type 17 (MRX17), a genetic disorder primarily affecting males.

Test Components

  • 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

Prior to undergoing the HSD17B10 Gene Mental Retardation X-linked Type 17 Genetic Test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session will be conducted to draw a pedigree chart of family members affected by MRX17.

Test Details

The HSD17B10 gene is associated with mental retardation, X-linked type 17 (MRX17). This genetic disorder primarily affects males and is characterized by intellectual disability, delayed speech and language development, and other cognitive impairments.

Our NGS (Next-Generation Sequencing) genetic testing utilizes advanced sequencing technologies to analyze multiple genes simultaneously. This comprehensive analysis of an individual’s genetic makeup allows us to identify any genetic variants or mutations that may be present.

In the context of MRX17, NGS genetic testing helps in identifying mutations or variants in the HSD17B10 gene that may be causing the condition. This information is crucial for confirming a diagnosis, understanding the underlying genetic cause, and providing appropriate genetic counseling and management strategies for affected individuals and their families.

Test Name HSD17B10 Gene Mental retardation X-linked type 17 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 HSD17B10 Gene Mental retardation, X-linked type 17 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with HSD17B10 Gene Mental retardation, X-linked type 17
Test Details

The HSD17B10 gene is associated with a condition called mental retardation, X-linked type 17 (MRX17). MRX17 is a genetic disorder that primarily affects males and is characterized by intellectual disability, delayed speech and language development, and other cognitive impairments.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic testing that uses advanced sequencing technologies to analyze multiple genes simultaneously. It allows for a comprehensive analysis of an individual’s genetic makeup, providing information about any genetic variants or mutations that may be present.

In the context of MRX17, NGS genetic testing can be used to identify mutations or variants in the HSD17B10 gene that may be causing the condition. This can help in confirming a diagnosis, understanding the underlying genetic cause, and providing appropriate genetic counseling and management strategies for affected individuals and their families.