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CDH15 Gene Mental Retardation Autosomal Dominant Type 3 Genetic Test

4,400 د.إ

-21%

The CDH15 gene is associated with a condition known as Mental Retardation, Autosomal Dominant Type 3 (MRD3), a disorder characterized by intellectual disabilities and possibly other neurological or physical abnormalities. The CDH15 gene plays a critical role in the development and function of the brain, influencing cell-cell adhesion processes which are essential for proper neural development.

A genetic test for MRD3 linked to the CDH15 gene can provide crucial information for individuals suspected of having this condition or families with a history of intellectual disabilities. This test involves analyzing the DNA to identify mutations in the CDH15 gene that are responsible for the disorder. Early diagnosis through genetic testing can aid in managing the condition more effectively, allowing for tailored educational programs, therapy, and support to improve the quality of life for affected individuals.

In the UAE, DNA Labs offers a comprehensive genetic test for the CDH15 gene to diagnose Mental Retardation, Autosomal Dominant Type 3. The test cost is set at 4400 AED, reflecting the specialized nature of the analysis and the advanced technology used to detect mutations in the gene accurately. Conducted in a state-of-the-art facility, the test provides a reliable diagnosis, enabling healthcare professionals and families to take informed steps towards managing the condition.

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CDH15 Gene Mental Retardation Autosomal Dominant Type 3 Genetic Test

At DNA Labs UAE, we offer the CDH15 Gene Mental Retardation Autosomal Dominant Type 3 Genetic Test to help diagnose and understand this genetic condition. This test is specifically designed for individuals with symptoms of mental retardation, autosomal dominant type 3 (MRD3).

Test Components and Price

  • Test Name: CDH15 Gene Mental Retardation Autosomal Dominant Type 3 Genetic Test
  • Price: 4400.0 AED

Sample Condition

We accept the following sample conditions for this test:

  • Blood
  • Extracted DNA
  • One drop of blood on FTA Card

Report Delivery

The test report will be delivered within 3 to 4 weeks after sample submission.

Method

We use NGS (Next-Generation Sequencing) technology for this genetic test. NGS allows us to analyze multiple genes simultaneously and identify mutations or variations associated with MRD3.

Test Type

This test specifically focuses on neurological disorders, including MRD3.

Doctor and Test Department

This test is conducted under the supervision of a neurologist and falls under the Genetics department.

Pre Test Information

Before undergoing the CDH15 Gene Mental Retardation Autosomal Dominant Type 3 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 MRD3.

Test Details

The CDH15 gene is associated with mental retardation, autosomal dominant type 3 (MRD3). This genetic condition is characterized by intellectual disability and other neurodevelopmental delays. The NGS genetic testing method allows for a more comprehensive analysis of the genetic factors contributing to MRD3 compared to traditional single-gene testing methods.

Test Name CDH15 Gene Mental retardation autosomal dominant type 3 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 CDH15 Gene Mental retardation, autosomal dominant type 3 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with CDH15 Gene Mental retardation, autosomal dominant type 3
Test Details

The CDH15 gene is associated with mental retardation, autosomal dominant type 3 (MRD3), which is a genetic condition characterized by intellectual disability and other neurodevelopmental delays. NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that can analyze multiple genes simultaneously to identify mutations or variations that may be associated with a specific condition, such as MRD3. This type of testing can provide a more comprehensive analysis of the genetic factors contributing to the condition compared to traditional single-gene testing methods.