MMAA Gene Methylmalonic Aciduria CblA Type Genetic Test sale cost 4400 AED
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MMAA Gene Methylmalonic Aciduria CblA Type Genetic Test Cost

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

-21%

The MMAA Gene Methylmalonic Aciduria CblA Type Genetic Test is a specialized diagnostic examination designed to detect mutations in the MMAA gene, which are responsible for a form of methylmalonic acidemia known as the cblA type. This rare genetic disorder disrupts the body’s ability to process certain fats and proteins, leading to the accumulation of methylmalonic acid in the blood. Symptoms can range from mild to severe and may include vomiting, dehydration, developmental delays, and more serious complications if left untreated.

Performed at DNA Labs UAE, this genetic test involves collecting a DNA sample, typically through a blood draw or cheek swab, to analyze the specific segments of the MMAA gene for any mutations. The test is crucial for early diagnosis and management of the condition, allowing for appropriate treatment plans to be developed, which can significantly improve the quality of life for affected individuals.

The cost of the MMAA Gene Methylmalonic Aciduria CblA Type Genetic Test at DNA Labs UAE is 4400 AED. This investment in health can provide essential information for families with a history of the disorder, or for those exhibiting symptoms, enabling early intervention and management of the condition.

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MMAA Gene Methylmalonic aciduria CblA type Genetic Test

In this blog post, we will discuss the details of the MMAA Gene Methylmalonic aciduria CblA type Genetic Test offered by DNA Labs UAE. This test is used to diagnose and understand the genetic factors associated with methylmalonic aciduria (MMA) type CblA.

Test Name: MMAA Gene Methylmalonic aciduria CblA 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:

Prior to undergoing the MMAA Gene Methylmalonic aciduria CblA type NGS Genetic DNA Test, it is important to provide the clinical history of the patient. Additionally, a Genetic Counselling session is recommended to draw a pedigree chart of family members affected by Methylmalonic aciduria CblA type.

Test Details:

The MMAA gene methylmalonic aciduria CblA type NGS genetic test is a genetic test that examines the MMAA gene for mutations associated with methylmalonic aciduria (MMA) type CblA. MMA is a rare inherited metabolic disorder characterized by the inability to break down certain proteins and fats, resulting in the accumulation of toxic substances in the body.

The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the MMAA gene. This helps identify any genetic variations or mutations that may be responsible for the condition.

Aside from diagnosing methylmalonic aciduria CblA type, this test can also be used for carrier screening or prenatal testing in families with a known history of the disorder. Identifying specific mutations in the MMAA gene can aid in understanding the underlying cause of the condition, providing valuable information for genetic counseling and potentially guiding treatment options.

It is important to note that this test should be performed and interpreted by a qualified healthcare professional or geneticist.

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

MMAA gene methylmalonic aciduria CblA type NGS genetic test is a genetic test that examines the MMAA gene for mutations associated with methylmalonic aciduria (MMA) type CblA. MMA is a rare inherited metabolic disorder characterized by the inability to break down certain proteins and fats, leading to the buildup of toxic substances in the body.

The NGS (Next-Generation Sequencing) technology used in this test allows for the simultaneous analysis of multiple genes, including the MMAA gene, to identify any genetic variations or mutations that may be responsible for the condition. This test helps in confirming a diagnosis of methylmalonic aciduria CblA type and can also be used for carrier screening or prenatal testing in families with a known history of the disorder.

Identifying specific mutations in the MMAA gene can aid in understanding the underlying cause of the condition, providing valuable information for genetic counseling and potentially guiding treatment options. It is important to note that this test should be performed and interpreted by a qualified healthcare professional or geneticist.

SKU: TEST-2536 Category:

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