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SMARCB1 Gene Mental Retardation Autosomal Dominant Type 15 Genetic Test

4,400 د.إ

-21%

The SMARCB1 Gene Mental Retardation Autosomal Dominant Type 15 Genetic Test is a specialized diagnostic procedure designed to detect mutations in the SMARCB1 gene, which are linked to the development of Mental Retardation, Autosomal Dominant Type 15 (MRD15). This condition is a neurodevelopmental disorder characterized by intellectual disability, delayed speech and motor milestones, and sometimes seizures and behavioral issues. The test involves analyzing the patient’s DNA, extracted from a blood sample, to identify any genetic alterations in the SMARCB1 gene that could be responsible for the disorder.

Performed at DNA Labs UAE, a leading facility in genetic testing, the test aims to provide conclusive genetic evidence for the diagnosis of MRD15, facilitating appropriate management and intervention strategies for affected individuals. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the SMARCB1 gene. This genetic test is crucial for families seeking answers to developmental delays and intellectual challenges in their loved ones, offering a path towards understanding and support tailored to the genetic makeup of the individual.

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SMARCB1 Gene Mental Retardation Autosomal Dominant Type 15 Genetic Test

Welcome to DNA Labs UAE, a leading genetic testing laboratory in the UAE. In this blog post, we will discuss the SMARCB1 Gene Mental Retardation Autosomal Dominant Type 15 Genetic Test, its components, cost, symptoms, diagnosis process, and more.

Test Details

The SMARCB1 gene is associated with a condition called mental retardation, autosomal dominant type 15 (MRD15). This condition is characterized by intellectual disability and developmental delay. NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. It allows for the detection of genetic variations or mutations that may be responsible for a particular condition. In the case of MRD15, NGS genetic testing can identify mutations in the SMARCB1 gene that may be causative or contribute to the condition. By performing NGS genetic testing, healthcare professionals can provide a more accurate diagnosis, assess the risk of passing the condition to future generations, and potentially guide treatment and management strategies for individuals with MRD15.

Test Name

SMARCB1 Gene Mental Retardation Autosomal Dominant Type 15 Genetic 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

Clinical History of Patient who is going for SMARCB1 Gene Mental Retardation, Autosomal Dominant Type 15 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with SMARCB1 Gene Mental Retardation, Autosomal Dominant Type 15.

Thank you for reading our blog post about the SMARCB1 Gene Mental Retardation Autosomal Dominant Type 15 Genetic Test. If you have any questions or would like to schedule a test, please contact DNA Labs UAE.

Test Name SMARCB1 Gene Mental retardation autosomal dominant type 15 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 SMARCB1 Gene Mental retardation, autosomal dominant type 15 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with SMARCB1 Gene Mental retardation, autosomal dominant type 15
Test Details

The SMARCB1 gene is associated with a condition called mental retardation, autosomal dominant type 15 (MRD15). This condition is characterized by intellectual disability and developmental delay.

NGS (Next-Generation Sequencing) genetic testing is a technique used to analyze multiple genes simultaneously. It allows for the detection of genetic variations or mutations that may be responsible for a particular condition. In the case of MRD15, NGS genetic testing can identify mutations in the SMARCB1 gene that may be causative or contribute to the condition.

By performing NGS genetic testing, healthcare professionals can provide a more accurate diagnosis, assess the risk of passing the condition to future generations, and potentially guide treatment and management strategies for individuals with MRD15.