MTR Gene Methylcobalamin Deficiency CblG Type Genetic Test
At DNA Labs UAE, we offer the MTR gene methylcobalamin deficiency CblG type genetic test. This test is designed to analyze the MTR gene for mutations or variations that may cause methylcobalamin deficiency CblG type. Methylcobalamin deficiency CblG type is a rare genetic disorder that affects the body’s ability to process vitamin B12, resulting in a deficiency of methylcobalamin.
Test Details
The MTR gene methylcobalamin deficiency CblG type NGS genetic test is performed using next-generation sequencing (NGS) technology. This allows us to examine the MTR gene and identify any genetic variations or mutations that may be associated with methylcobalamin deficiency CblG type. The test can be performed on a blood or saliva sample.
Components
- Test Name: MTR Gene Methylcobalamin Deficiency CblG Type Genetic Test
- Price: 3200.0 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, Genetic Counselling Session
Symptoms and Diagnosis
Methylcobalamin deficiency CblG type can present with various symptoms, including neurological problems, developmental delays, and megaloblastic anemia. Diagnosis of this condition involves analyzing the MTR gene for mutations or variations using the MTR gene methylcobalamin deficiency CblG type genetic test.
Treatment and Management
Once a diagnosis is made, healthcare professionals can provide appropriate treatment and management strategies for individuals with methylcobalamin deficiency CblG type. This may include dietary changes, supplementation of vitamin B12, and other supportive measures.
Importance of Genetic Testing
The MTR gene methylcobalamin deficiency CblG type NGS genetic test is crucial in determining the underlying cause of methylcobalamin deficiency. It helps healthcare professionals understand the genetic basis of the condition, which can guide treatment decisions and provide valuable information for families affected by this genetic disorder.
Please note that this test specifically focuses on methylcobalamin deficiency CblG type caused by mutations in the MTR gene. Other types of methylcobalamin deficiency may be caused by mutations in different genes, so additional genetic testing may be necessary to fully understand the genetic basis of methylcobalamin deficiency in an individual.
| Test Name | MTR Gene Methylcobalamin deficiency CblG type Genetic Test |
|---|---|
| Components | |
| Price | 3200.0 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 MTR Gene Methylcobalamin deficiency CblG type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Methylcobalamin deficiency CblG type |
| Test Details |
MTR gene methylcobalamin deficiency CblG type NGS genetic test is a type of genetic test that analyzes the MTR gene for mutations or variations that may cause methylcobalamin deficiency CblG type. Methylcobalamin deficiency CblG type is a rare genetic disorder that affects the body’s ability to process vitamin B12, leading to a deficiency of methylcobalamin, a form of vitamin B12. The test uses next-generation sequencing (NGS) technology to examine the MTR gene and identify any genetic variations or mutations that may be associated with methylcobalamin deficiency CblG type. This information can help healthcare professionals diagnose the condition and provide appropriate treatment and management strategies. The MTR gene is responsible for producing an enzyme called methionine synthase, which plays a crucial role in the conversion of homocysteine to methionine. Mutations or variations in the MTR gene can impair the function of this enzyme, leading to the accumulation of homocysteine and a deficiency of methylcobalamin. The MTR gene methylcobalamin deficiency CblG type NGS genetic test can be performed on a blood or saliva sample. The sample is sent to a laboratory where DNA sequencing is performed to analyze the MTR gene. The results of the test can help determine the underlying cause of methylcobalamin deficiency and guide treatment decisions. It is important to note that this test is specific to methylcobalamin deficiency CblG type caused by mutations in the MTR gene. There are other types of methylcobalamin deficiency that may be caused by mutations in different genes. Therefore, additional genetic testing may be necessary to fully understand the genetic basis of methylcobalamin deficiency in an individual. |
