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SMARCA4 Gene Mental Retardation Autosomal Dominant Type 16 Genetic Test

4,400 د.إ

-21%

The SMARCA4 Gene Mental Retardation Autosomal Dominant Type 16 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the SMARCA4 gene that are associated with Autosomal Dominant Mental Retardation Type 16. This condition is a genetic disorder characterized by intellectual disability and possibly other neurological or physical abnormalities. The test is crucial for families with a history of this condition, as it can provide definitive answers regarding the genetic status of family members, guide clinical management, and inform reproductive decisions.

Performed using a sample of the patient’s blood or saliva, the test specifically looks for alterations in the SMARCA4 gene, which plays a significant role in chromatin remodeling and is essential for normal brain development. Identifying mutations in this gene can help in understanding the cause of the intellectual disability and in some cases, guide therapeutic and educational interventions.

The cost of the test is 4400 AED, reflecting the comprehensive analysis and the specialized expertise required to interpret the results. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test adheres to stringent quality controls, ensuring accuracy and reliability of the results. Families undergoing this testing can expect professional guidance throughout the process, from pre-test counseling to understand the implications of the test, through to post-test support to discuss the results and their implications.

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SMARCA4 Gene Mental Retardation Autosomal Dominant Type 16 Genetic Test

At DNA Labs UAE, we offer the SMARCA4 Gene Mental Retardation Autosomal Dominant Type 16 Genetic Test. This test is designed to diagnose individuals with mental retardation caused by a mutation in the SMARCA4 gene.

Test Details

The SMARCA4 gene is associated with mental retardation, autosomal dominant type 16. This condition is characterized by intellectual disability and developmental delays. Our NGS (Next-Generation Sequencing) genetic testing method allows us to analyze the DNA sequence of the SMARCA4 gene and identify any variations or mutations that may be present.

NGS testing involves sequencing large amounts of DNA in a rapid and cost-effective manner. It can provide a comprehensive analysis of the entire gene, allowing for the detection of various types of mutations, including single nucleotide variants, insertions, deletions, and rearrangements.

By identifying the specific mutation in the SMARCA4 gene, NGS testing can help in understanding the underlying genetic cause of mental retardation in an individual. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options in the future.

It’s important to note that NGS testing is typically performed by a healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance based on the individual’s specific situation.

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 SMARCA4 Gene Mental Retardation Autosomal Dominant Type 16 NGS Genetic DNA Test, it is recommended to provide the following:

  • Clinical History of the patient who is going for the test
  • A Genetic Counselling session to draw a pedigree chart of family members affected with SMARCA4 Gene Mental Retardation Autosomal Dominant Type 16

For more information or to schedule an appointment, please contact our Genetics department.

Test Name SMARCA4 Gene Mental retardation autosomal dominant type 16 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 SMARCA4 Gene Mental retardation, autosomal dominant type 16 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SMARCA4 Gene Mental retardation, autosomal dominant type 16
Test Details

The SMARCA4 gene is associated with mental retardation, autosomal dominant type 16. This condition is characterized by intellectual disability and developmental delays.

NGS (Next-Generation Sequencing) genetic testing can be used to analyze the DNA sequence of the SMARCA4 gene and identify any variations or mutations that may be present. This can help in diagnosing individuals with mental retardation and determining if it is caused by a mutation in the SMARCA4 gene.

NGS testing involves sequencing large amounts of DNA in a rapid and cost-effective manner. It can provide a comprehensive analysis of the entire gene, allowing for the detection of various types of mutations, including single nucleotide variants, insertions, deletions, and rearrangements.

By identifying the specific mutation in the SMARCA4 gene, NGS testing can help in understanding the underlying genetic cause of mental retardation in an individual. This information can be useful for genetic counseling, family planning, and potentially guiding treatment options in the future.

It’s important to note that NGS testing is typically performed by a healthcare professional or genetic counselor, who can interpret the results and provide appropriate guidance based on the individual’s specific situation.