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MLYCD Gene Malonyl-CoA Decarboxylase Deficiency Genetic Test Cost

Original price was: 5,600 د.إ.Current price is: 3,200 د.إ.

-43%

The MLYCD Gene Malonyl-CoA Decarboxylase Deficiency Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the MLYCD gene. These mutations are responsible for Malonyl-CoA decarboxylase deficiency, a rare genetic disorder that affects the body’s ability to metabolize certain fats, leading to a buildup of malonic acid and other harmful substances. Symptoms of the disorder can vary but often include developmental delays, hypoglycemia, and cardiomyopathy, among others.

The test, priced at 3200 AED, involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab. The sample is then analyzed in the laboratory using advanced genetic sequencing techniques to detect any abnormalities or mutations in the MLYCD gene. The results of this test can provide crucial information for the diagnosis and management of Malonyl-CoA decarboxylase deficiency, enabling targeted treatment plans and genetic counseling for affected families. DNA Labs UAE is equipped with state-of-the-art facilities and experienced professionals to ensure accurate and reliable testing outcomes.

Description

Genetic Lab Blog – MLYCD Gene Malonyl-CoA decarboxylase deficiency Genetic Test cost AED:3200.0 symptoms diagnosis

At DNA Labs UAE, we offer the MLYCD Gene Malonyl-CoA decarboxylase deficiency Genetic Test for individuals who may be affected by this rare genetic disorder. The test is priced at 3200.0 AED and can be conducted using a blood sample, extracted DNA, or one drop of blood on an FTA card.

Once the sample is collected, the report delivery time is approximately 3 to 4 weeks. The test utilizes NGS (Next-Generation Sequencing) technology, which allows for the simultaneous analysis of multiple genes or even the entire genome.

The MLYCD gene is responsible for encoding the enzyme Malonyl-CoA decarboxylase. MLYCD deficiency is characterized by impaired function of this enzyme. NGS genetic testing can identify mutations or variations in the MLYCD gene that may be responsible for the condition.

By sequencing the MLYCD gene, NGS testing can detect mutations or variations that may affect the enzyme’s structure or function, leading to a deficiency. This information is crucial for diagnosis, determining the mode of inheritance, and providing genetic counseling for affected individuals and their families.

NGS genetic testing is a more comprehensive and efficient approach compared to traditional sequencing methods, as it can analyze multiple genes simultaneously. This is particularly beneficial when the genetic cause of a condition is not well-known or when multiple genes may be involved in the disease pathogenesis.

It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors. These professionals can provide appropriate guidance and support to individuals undergoing testing.

If you or a family member has a clinical history of Malonyl-CoA decarboxylase deficiency or suspect that you may be affected by this condition, we recommend scheduling a genetic counseling session. During this session, a pedigree chart of affected family members can be drawn to better understand the inheritance pattern and assess the need for genetic testing.

At DNA Labs UAE, we are dedicated to providing accurate and reliable genetic testing services. Contact us today to learn more about the MLYCD Gene Malonyl-CoA decarboxylase deficiency Genetic Test and how it can benefit you and your family.

Test Name	MLYCD Gene Malonyl-CoA decarboxylase deficiency 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 MLYCD Gene Malonyl-CoA decarboxylase deficiency NGS Genetic DNA Test A Genetic Counselling session to draw a pedigree chart of family members affected with Malonyl-CoA decarboxylase deficiency
Test Details	MLYCD gene refers to the gene that encodes for the enzyme Malonyl-CoA decarboxylase. Malonyl-CoA decarboxylase deficiency (MLYCD deficiency) is a rare genetic disorder characterized by the impaired function of this enzyme. NGS (Next-Generation Sequencing) genetic testing is a high-throughput DNA sequencing technology that allows the simultaneous analysis of multiple genes or even the entire genome. In the context of MLYCD deficiency, NGS genetic testing can be used to identify mutations or variations in the MLYCD gene that may be responsible for the condition. By sequencing the MLYCD gene, NGS testing can detect mutations or variations that may affect the enzyme’s structure or function, leading to a deficiency. This information can be used for diagnosis, determining the mode of inheritance, and providing genetic counseling for affected individuals and their families. NGS genetic testing offers a more comprehensive and efficient approach compared to traditional sequencing methods, as it can analyze multiple genes simultaneously. This can be particularly beneficial in cases where the genetic cause of a condition is not well-known or when multiple genes may be involved in the disease pathogenesis. It is important to note that NGS genetic testing should be performed and interpreted by qualified healthcare professionals, such as geneticists or genetic counselors, who can provide appropriate guidance and support to individuals undergoing testing.