IDH2 Gene D-2-hydroxyglutaric aciduria type 2 Genetic Test
Welcome to DNA Labs UAE, where we offer the IDH2 Gene D-2-hydroxyglutaric aciduria type 2 Genetic Test. This test is designed to analyze the IDH2 gene, which is responsible for producing the isocitrate dehydrogenase 2 enzyme. Mutations in this gene can lead to D-2-hydroxyglutaric aciduria type 2, a rare genetic disorder affecting the metabolism of D-2-hydroxyglutaric acid.
Test Details
The IDH2 Gene D-2-hydroxyglutaric aciduria type 2 Genetic Test is a comprehensive analysis of the genetic code using NGS (Next-Generation Sequencing) technology. This advanced sequencing technology allows us to simultaneously analyze multiple genes, including the IDH2 gene and other genes associated with D-2-hydroxyglutaric aciduria type 2.
Cost and Components
The cost of the IDH2 Gene D-2-hydroxyglutaric aciduria type 2 Genetic Test is AED 4400.0. The test requires a blood sample, extracted DNA, or one drop of blood on an FTA card as the sample condition.
Report Delivery and Method
After the sample is collected, the report will be delivered within 3 to 4 weeks. The NGS technology is used to analyze the sample and identify any mutations or variations in the IDH2 gene.
Symptoms and Diagnosis
D-2-hydroxyglutaric aciduria type 2 is characterized by the buildup of D-2-hydroxyglutaric acid in the body. This can lead to various symptoms, including developmental delay, intellectual disability, seizures, movement disorders, and abnormalities in the brain. If a healthcare provider suspects D-2-hydroxyglutaric aciduria type 2 based on a patient’s symptoms, they may recommend the IDH2 Gene D-2-hydroxyglutaric aciduria type 2 Genetic Test to confirm the diagnosis.
Doctor and Test Department
The IDH2 Gene D-2-hydroxyglutaric aciduria type 2 Genetic Test is typically ordered by a general physician and falls under the genetics test department.
Pre Test Information
Prior to the test, it is important to provide the clinical history of the patient. Additionally, a genetic counseling session may be conducted to draw a pedigree chart of family members affected with D-2-hydroxyglutaric aciduria type 2. This information helps in understanding the inheritance pattern and assessing the risk of the condition in other family members.
Conclusion
The IDH2 Gene D-2-hydroxyglutaric aciduria type 2 Genetic Test offered by DNA Labs UAE is a valuable tool for diagnosing this rare genetic disorder. By analyzing the IDH2 gene and other associated genes, this test can provide important information for treatment decisions and genetic counseling. If you suspect D-2-hydroxyglutaric aciduria type 2 or have a family history of the condition, consider getting tested today.
| Test Name | IDH2 Gene D-2-hydroxyglutaric aciduria type 2 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 | Metabolic Disorders |
| Doctor | General Physician |
| Test Department: | Genetics |
| Pre Test Information | Clinical History of Patient who is going for IDH2 Gene D-2-hydroxyglutaric aciduria type 2 NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with D-2-hydroxyglutaric aciduria type 2 |
| Test Details |
The IDH2 gene is responsible for providing instructions to make an enzyme called isocitrate dehydrogenase 2. Mutations in this gene can lead to a condition called D-2-hydroxyglutaric aciduria type 2. D-2-hydroxyglutaric aciduria type 2 is a rare genetic disorder that affects the metabolism of a specific type of acid called D-2-hydroxyglutaric acid. This condition is characterized by the buildup of this acid in the body, leading to a range of symptoms including developmental delay, intellectual disability, seizures, movement disorders, and abnormalities in the brain. NGS (Next-Generation Sequencing) Genetic Testing is a type of genetic test that uses advanced sequencing technologies to analyze multiple genes simultaneously. This type of testing can be used to identify mutations or variations in the IDH2 gene, as well as other genes that may be associated with D-2-hydroxyglutaric aciduria type 2. NGS allows for a more comprehensive analysis of the genetic code, making it a powerful tool for diagnosing genetic disorders. If a healthcare provider suspects D-2-hydroxyglutaric aciduria type 2 based on a patient’s symptoms, they may recommend an NGS genetic test to confirm the diagnosis. This test typically involves taking a sample of the patient’s DNA, usually through a blood sample, and analyzing it in a laboratory. The results of the test can help guide treatment decisions and provide valuable information for genetic counseling. |
