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MMADHC Gene Methylmalonic Aciduria CblD Type Genetic Test Cost

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

-21%

The MMADHC Gene Methylmalonic Aciduria CblD Type Genetic Test is a specialized diagnostic tool aimed at identifying mutations in the MMADHC gene, which are associated with a rare inherited disorder known as Methylmalonic Aciduria CblD Type. This condition is part of a group of metabolic disorders that affect the body’s ability to process certain parts of proteins and fats properly, leading to a buildup of toxic substances in the body. Symptoms can vary widely among affected individuals but may include developmental delay, intellectual disability, failure to thrive, and various metabolic complications.

Performed at DNA Labs UAE, this genetic test involves analyzing the patient’s DNA to detect mutations in the MMADHC gene that could lead to the development of Methylmalonic Aciduria CblD Type. The process is comprehensive, ensuring high accuracy in the diagnosis, which is crucial for managing the condition effectively and providing appropriate treatment options.

The cost of the MMADHC Gene Methylmalonic Aciduria CblD Type Genetic Test is 4400 AED. Although the price may seem high, the test provides invaluable insights into the genetic makeup of individuals suspected of having this condition, enabling early intervention and personalized management strategies to improve quality of life and outcomes.

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MMADHC Gene Methylmalonic aciduria CblD type Genetic Test

Are you concerned about the possibility of having Methylmalonic aciduria CblD type? DNA Labs UAE offers the MMADHC Gene Methylmalonic aciduria CblD type Genetic Test to help you find answers. This blog will provide you with all the details you need to know about this test.

Test Details

The MMADHC gene is responsible for providing instructions for the production of a protein called methylmalonic aciduria and homocystinuria type D protein. Mutations in this gene can lead to a condition known as methylmalonic aciduria CblD type. Methylmalonic aciduria CblD type is an inherited metabolic disorder that affects the body’s ability to break down certain proteins and fats. This leads to the buildup of toxic substances in the body, causing a range of symptoms including developmental delay, intellectual disability, seizures, vision problems, and anemia.

Test Components

The MMADHC Gene Methylmalonic aciduria CblD type Genetic Test includes the following components:

  • Test Name: MMADHC Gene Methylmalonic aciduria CblD type Genetic Test
  • 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 MMADHC Gene Methylmalonic aciduria CblD type NGS Genetic DNA Test. A Genetic Counselling session to draw a pedigree chart of family members affected with Methylmalonic aciduria CblD type.

What is NGS Genetic Testing?

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to examine the DNA sequence of specific genes. In the case of methylmalonic aciduria CblD type, NGS genetic testing can identify mutations in the MMADHC gene that may be responsible for the condition. This type of genetic testing can help diagnose individuals with methylmalonic aciduria CblD type, provide information about the specific genetic mutation causing the condition, and guide treatment and management options. It can also be used for carrier testing in individuals with a family history of the condition.

It is important to note that genetic testing should be conducted under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.

Don’t let the uncertainty of your genetic makeup hold you back. Contact DNA Labs UAE today to schedule your MMADHC Gene Methylmalonic aciduria CblD type Genetic Test and take control of your health.

Test Name MMADHC Gene Methylmalonic aciduria CblD type 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 MMADHC Gene Methylmalonic aciduria CblD type NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Methylmalonic aciduria CblD type
Test Details

The MMADHC gene is responsible for providing instructions for the production of a protein called methylmalonic aciduria and homocystinuria type D protein. Mutations in this gene can lead to a condition known as methylmalonic aciduria CblD type.

Methylmalonic aciduria CblD type is an inherited metabolic disorder that affects the body’s ability to break down certain proteins and fats. This leads to the buildup of toxic substances in the body, causing a range of symptoms including developmental delay, intellectual disability, seizures, vision problems, and anemia.

NGS (Next-Generation Sequencing) genetic testing is a type of genetic test that uses advanced sequencing technology to examine the DNA sequence of specific genes. In the case of methylmalonic aciduria CblD type, NGS genetic testing can identify mutations in the MMADHC gene that may be responsible for the condition.

This type of genetic testing can help diagnose individuals with methylmalonic aciduria CblD type, provide information about the specific genetic mutation causing the condition, and guide treatment and management options. It can also be used for carrier testing in individuals with a family history of the condition.

It is important to note that genetic testing should be conducted under the guidance of a healthcare professional or genetic counselor who can provide appropriate counseling and interpretation of the results.

SKU: TEST-2539 Category:

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