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. |