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GRIN1 Gene Mental Retardation Autosomal Dominant Type 8 Genetic Test

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

-21%

The “GRIN1 Gene Mental Retardation Autosomal Dominant Type 8 Genetic Test” is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the GRIN1 gene. These mutations are associated with Mental Retardation, Autosomal Dominant Type 8, a rare genetic disorder characterized by intellectual disability and possibly other neurological or developmental issues. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing the genetic material for specific abnormalities within the GRIN1 gene. With a cost of 4400 AED, this test is a crucial tool for families seeking answers to developmental delays or intellectual challenges, providing them with vital information for managing and understanding their condition. It also plays a significant role in guiding treatment plans and interventions, offering a clearer prognosis for affected individuals.

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GRIN1 Gene Mental Retardation Autosomal Dominant Type 8 Genetic Test

Test Name: GRIN1 Gene Mental Retardation Autosomal Dominant Type 8 Genetic Test

Components: Blood or Extracted DNA or One drop Blood on FTA Card

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 GRIN1 Gene Mental Retardation, Autosomal Dominant Type 8 NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with GRIN1 Gene Mental Retardation, Autosomal Dominant Type 8.

Test Details

The GRIN1 gene is associated with a condition called Mental Retardation, Autosomal Dominant Type 8 (MRD8). This condition is characterized by intellectual disability, delayed development, and other neurological abnormalities.

NGS Genetic Test refers to Next-Generation Sequencing, a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the case of MRD8, an NGS genetic test can be used to sequence the GRIN1 gene to identify any mutations or variants that may be causing the condition.

By identifying specific genetic changes in the GRIN1 gene, an NGS genetic test can help confirm a diagnosis of MRD8 and provide important information for genetic counseling, management, and treatment of affected individuals and their families. It can also be used for carrier testing and prenatal diagnosis in families with a known history of MRD8.

Test Name GRIN1 Gene Mental retardation autosomal dominant type 8 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 GRIN1 Gene Mental retardation, autosomal dominant type 8 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with GRIN1 Gene Mental retardation, autosomal dominant type 8
Test Details

The GRIN1 gene is associated with a condition called Mental retardation, autosomal dominant type 8 (MRD8). This condition is characterized by intellectual disability, delayed development, and other neurological abnormalities.

NGS Genetic Test refers to Next-Generation Sequencing, a high-throughput DNA sequencing technology that can analyze multiple genes simultaneously. In the case of MRD8, an NGS genetic test can be used to sequence the GRIN1 gene to identify any mutations or variants that may be causing the condition.

By identifying specific genetic changes in the GRIN1 gene, an NGS genetic test can help confirm a diagnosis of MRD8 and provide important information for genetic counseling, management, and treatment of affected individuals and their families. It can also be used for carrier testing and prenatal diagnosis in families with a known history of MRD8.