Sale!

MCEE Gene Methylmalonyl-CoA Epimerase Deficiency Genetic Test Cost

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

-21%

The MCEE Gene Methylmalonyl-CoA Epimerase Deficiency Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the MCEE gene, which can lead to Methylmalonyl-CoA Epimerase deficiency. This condition is a rare metabolic disorder that affects the body’s ability to convert certain fats and proteins into energy, leading to a buildup of harmful substances in the body. Early detection through genetic testing is crucial for managing symptoms and preventing severe complications.

Performed at DNA Labs UAE, the test involves analyzing the patient’s DNA to look for specific genetic alterations associated with the disorder. The process is meticulous, ensuring accurate and reliable results that can guide treatment and management strategies for affected individuals.

The cost of the MCEE Gene Methylmalonyl-CoA Epimerase Deficiency Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to detect any mutations in the MCEE gene, providing essential information for patients and their families to address this metabolic disorder effectively.

Description

MCEE Gene Methylmalonyl-CoA epimerase deficiency Genetic Test

At DNA Labs UAE, we offer the MCEE Gene Methylmalonyl-CoA epimerase deficiency Genetic Test to help diagnose and identify mutations or variations in the MCEE gene. This test is essential for individuals who exhibit symptoms of methylmalonyl-CoA epimerase deficiency or have a family history of the disorder.

Test Details

The MCEE gene methylmalonyl-CoA epimerase deficiency NGS genetic test is a diagnostic test that uses Next-Generation Sequencing (NGS) technology to analyze the entire MCEE gene sequence. This gene is responsible for encoding the enzyme methylmalonyl-CoA epimerase, which plays a crucial role in the breakdown of certain amino acids and fatty acids.

Methylmalonyl-CoA epimerase deficiency is a rare genetic disorder that affects the body’s ability to process certain amino acids and fatty acids properly. It can lead to the accumulation of toxic substances in the body, causing various symptoms such as developmental delays, intellectual disability, seizures, and metabolic acidosis.

The MCEE Gene Methylmalonyl-CoA epimerase deficiency Genetic Test is performed using a blood sample or extracted DNA. Alternatively, one drop of blood can be collected on an FTA card. The test results are typically delivered within 3 to 4 weeks.

Test Cost

The cost of the MCEE Gene Methylmalonyl-CoA epimerase deficiency Genetic Test is AED 4400.0.

Doctor and Test Department

This test is ordered by a General Physician and is performed in our Genetics department.

Pre Test Information

Prior to the test, it is important to provide the patient’s clinical history. Additionally, a Genetic Counselling session may be conducted to draw a pedigree chart of family members affected with Methylmalonyl-CoA epimerase deficiency.

Interpreting the Test Results

The results of the MCEE Gene Methylmalonyl-CoA epimerase deficiency Genetic Test should be interpreted by a qualified geneticist or genetic counselor. It is important to consider the individual’s clinical symptoms and other diagnostic tests to make an accurate diagnosis.

At DNA Labs UAE, we are dedicated to providing accurate and personalized genetic testing services. Contact us today to learn more about the MCEE Gene Methylmalonyl-CoA epimerase deficiency Genetic Test and how it can help in the diagnosis and treatment of this rare genetic disorder.

Test Name	MCEE Gene Methylmalonyl-CoA epimerase deficiency 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 MCEE Gene Methylmalonyl-CoA epimerase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Methylmalonyl-CoA epimerase deficiency
Test Details	MCEE gene methylmalonyl-CoA epimerase deficiency NGS genetic test is a diagnostic test used to detect mutations or variations in the MCEE gene. This gene is responsible for encoding the enzyme methylmalonyl-CoA epimerase, which plays a crucial role in the breakdown of certain amino acids and fatty acids. Methylmalonyl-CoA epimerase deficiency is a rare genetic disorder that affects the body’s ability to process certain amino acids and fatty acids properly. It can lead to the accumulation of toxic substances in the body, causing various symptoms such as developmental delays, intellectual disability, seizures, and metabolic acidosis. The NGS (Next-Generation Sequencing) genetic test is a highly advanced and accurate method used to analyze the entire MCEE gene sequence. It can identify any mutations, deletions, or insertions in the gene that may be responsible for the deficiency. This genetic test is typically performed on individuals who exhibit symptoms of methylmalonyl-CoA epimerase deficiency or have a family history of the disorder. The results of the test can help healthcare professionals make an accurate diagnosis and develop a personalized treatment plan for the affected individual. It is important to note that this test may not be available in all healthcare facilities and should be performed by a qualified geneticist or genetic counselor. Additionally, the test results should be interpreted in conjunction with the individual’s clinical symptoms and other diagnostic tests to make an accurate diagnosis.

Browse

Want to chat?

Social