CD320 Gene Methylmalonic aciduria CblR type Genetic Test
At DNA Labs UAE, we offer the CD320 Gene Methylmalonic aciduria CblR type Genetic Test. This test is used to identify mutations or variations in the CD320 gene that are associated with methylmalonic aciduria CblR type, a rare inherited metabolic disorder.
Test Components
The CD320 Gene Methylmalonic aciduria CblR type Genetic Test includes:
- NGS Technology
Price
The cost of the CD320 Gene Methylmalonic aciduria CblR type Genetic Test is 3200.0 AED.
Sample Condition
We accept the following sample conditions for this test:
- Blood
- Extracted DNA
- One drop of blood on FTA Card
Report Delivery
The report for the CD320 Gene Methylmalonic aciduria CblR type Genetic Test will be delivered within 3 to 4 weeks.
Test Method
The CD320 Gene Methylmalonic aciduria CblR type Genetic Test utilizes NGS (Next-Generation Sequencing) technology.
Test Type
This test is categorized under Metabolic Disorders.
Doctor
The CD320 Gene Methylmalonic aciduria CblR type Genetic Test can be ordered by a General Physician.
Test Department
This test is conducted by our Genetics department.
Pre Test Information
Prior to undergoing the CD320 Gene Methylmalonic aciduria CblR type Genetic Test, it is important to provide the following information:
- Clinical History of the patient who is going for the test
- A Genetic Counselling session to draw a pedigree chart of family members affected with Methylmalonic aciduria CblR type
Test Details
The CD320 gene methylmalonic aciduria CblR type NGS genetic test is a type of genetic test used to identify mutations or variations in the CD320 gene associated with methylmalonic aciduria CblR type. Methylmalonic aciduria CblR type is a rare inherited metabolic disorder characterized by the inability to properly process vitamin B12, resulting in the accumulation of toxic substances in the body.
The NGS technology used in this genetic test allows for the simultaneous analysis of multiple genes, including the CD320 gene, to detect any genetic variations or mutations. This test aids in the diagnosis of methylmalonic aciduria CblR type and provides essential information for the management and treatment of affected individuals.
The CD320 gene encodes a receptor protein involved in the cellular uptake of vitamin B12. Mutations or variations in this gene can disrupt the normal functioning of the receptor protein, leading to impaired processing of vitamin B12 and the development of methylmalonic aciduria CblR type.
The genetic test typically involves obtaining a DNA sample, usually through a blood or saliva sample, from the individual being tested. The DNA is then analyzed using NGS technology to identify any mutations or variations in the CD320 gene.
The results of the test can confirm a diagnosis of methylmalonic aciduria CblR type and guide appropriate treatment and management strategies. It is important to note that this genetic test is typically ordered by a healthcare professional, such as a geneticist or a metabolic specialist, who will interpret the results and provide appropriate counseling and guidance based on the findings.
Genetic testing can have significant implications for individuals and their families. Therefore, it is recommended to seek professional advice and support when considering or undergoing genetic testing.
Test Name | CD320 Gene Methylmalonic aciduria CblR 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 CD320 Gene Methylmalonic aciduria CblR type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Methylmalonic aciduria CblR type |
Test Details |
CD320 gene methylmalonic aciduria CblR type NGS genetic test is a type of genetic test that is used to identify mutations or variations in the CD320 gene that are associated with methylmalonic aciduria CblR type. Methylmalonic aciduria CblR type is a rare inherited metabolic disorder characterized by the inability to properly process vitamin B12, leading to the buildup of toxic substances in the body. The NGS (Next-Generation Sequencing) technology used in this genetic test allows for the simultaneous analysis of multiple genes, including the CD320 gene, to detect any genetic variations or mutations. This test can help in the diagnosis of methylmalonic aciduria CblR type and provide important information for the management and treatment of affected individuals. The CD320 gene encodes a receptor protein that is involved in the cellular uptake of vitamin B12. Mutations or variations in this gene can disrupt the normal functioning of the receptor protein, leading to the impaired processing of vitamin B12 and the development of methylmalonic aciduria CblR type. The genetic test typically involves obtaining a DNA sample, usually through a blood or saliva sample, from the individual being tested. The DNA is then analyzed using NGS technology to identify any mutations or variations in the CD320 gene. The results of the test can help confirm a diagnosis of methylmalonic aciduria CblR type and guide appropriate treatment and management strategies. It is important to note that this genetic test is typically ordered by a healthcare professional, such as a geneticist or a metabolic specialist, who will interpret the results and provide appropriate counseling and guidance based on the findings. Genetic testing can have important implications for individuals and their families, and it is recommended to seek professional advice and support when considering or undergoing genetic testing. |