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UPF3B Gene Mental Retardation X-Linked Type 14 Genetic Test

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

-21%

The UPF3B Gene Mental Retardation X-Linked Type 14 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the UPF3B gene, which is located on the X chromosome. This gene plays a critical role in the nonsense-mediated mRNA decay pathway, which is essential for normal brain development and function. Mutations in the UPF3B gene have been linked to various neurodevelopmental disorders, including intellectual disability, autism spectrum disorders, and schizophrenia. These conditions are often referred to collectively as X-linked mental retardation type 14.

The test is particularly valuable for families with a history of X-linked intellectual disabilities, providing crucial information for genetic counseling, early intervention, and personalized management plans for affected individuals. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific mutations in the UPF3B gene.

The cost of the UPF3B Gene Mental Retardation X-Linked Type 14 Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated technology and expert analysis required to accurately identify mutations in the UPF3B gene. Patients considering this test are advised to consult with a genetic counselor or healthcare provider to understand the implications of the results and the best course of action based on the findings.

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UPF3B Gene Mental Retardation X-linked Type 14 Genetic Test

At DNA Labs UAE, we offer the UPF3B Gene Mental Retardation X-linked Type 14 Genetic Test to diagnose and provide information about this genetic disorder. This test is specifically designed to analyze the UPF3B gene, which is associated with mental retardation, X-linked type 14 (MRX14).

MRX14 primarily affects males and is characterized by intellectual disability, delayed speech development, behavioral problems, and sometimes physical abnormalities. To determine if a patient has MRX14, we use NGS (Next-Generation Sequencing) technology to analyze their DNA for any mutations or abnormalities in the UPF3B gene.

Test Details

  • Test Name: UPF3B Gene Mental Retardation X-linked Type 14 Genetic Test
  • Components: Blood or Extracted DNA or One drop Blood on FTA Card
  • Price: 4400.0 AED
  • 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 UPF3B Gene Mental Retardation, X-linked type 14 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with UPF3B Gene Mental Retardation, X-linked type 14

NGS genetic testing for UPF3B gene mutations can help in diagnosing MRX14 and providing information about the genetic cause of the disorder. It can also be used for carrier testing in females who may be at risk of passing on the mutation to their children. However, it is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.

Test Name UPF3B Gene Mental retardation X-linked type 14 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 UPF3B Gene Mental retardation, X-linked type 14 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with UPF3B Gene Mental retardation, X-linked type 14
Test Details

The UPF3B gene is associated with mental retardation, X-linked type 14 (MRX14), which is a genetic disorder that primarily affects males. This disorder is characterized by intellectual disability, delayed speech development, behavioral problems, and sometimes physical abnormalities.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the UPF3B gene and identify any mutations or abnormalities that may be present. This type of testing involves sequencing the individual’s DNA to identify variations in the gene sequence that may be associated with the disorder.

NGS genetic testing for UPF3B gene mutations can help in diagnosing MRX14 and providing information about the genetic cause of the disorder. It can also be used for carrier testing in females who may be at risk of passing on the mutation to their children.

It is important to note that genetic testing should be done under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.