MTR Gene Methylcobalamin Deficiency CblG Type Genetic Test sale cost 3200 AED

MTR Gene Methylcobalamin Deficiency CblG Type Genetic Test Cost

The "MTR Gene Methylcobalamin Deficiency CblG Type Genetic Test" is a specialized diagnostic tool designed to identify mutations in the MTR gene, which can lead to a rare form of Methylcobalamin deficiency known as CblG type. Methylcobalamin is a form of vitamin B12 that is crucial for various bodily functions, including DNA synthesis and neurological health. Deficiencies in this vital nutrient due to genetic mutations can lead to a range of health issues, including developmental delays, neurological problems, and hematological disorders. This genetic test is performed to confirm a suspected diagnosis, allowing for early intervention and management of the condition. By analyzing the DNA, specifically targeting the MTR gene, healthcare providers can identify mutations that are responsible for the CblG type of Methylcobalamin deficiency. This precise approach enables tailored treatment plans that can significantly improve patient outcomes. The test is available at DNA Labs UAE, a leading facility in genetic testing and diagnostics. The cost of the test is 3200 AED, reflecting the advanced technology and expertise required to accurately identify the specific gene mutations. Through this test, patients and their families can gain crucial information for managing the condition, guiding dietary and medical interventions to mitigate the impact of the deficiency.
ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency Genetic Test sale cost 4400 AED

ALDH6A1 Gene Methylmalonate Semialdehyde Dehydrogenase Deficiency Genetic Test Cost

The ALDH6A1 gene plays a critical role in amino acid metabolism, specifically in the breakdown process of certain amino acids. A deficiency in the enzyme methylmalonate semialdehyde dehydrogenase, which is encoded by the ALDH6A1 gene, can lead to a rare metabolic disorder. This condition can result in various health issues, including developmental delays, neurological problems, and metabolic imbalances. To diagnose this deficiency, a genetic test is available at DNA Labs UAE. This test specifically looks for mutations in the ALDH6A1 gene that are known to cause the enzyme deficiency. By analyzing a patient's DNA, the test can confirm whether the individual has the genetic mutation responsible for the condition. The cost of the ALDH6A1 gene methylmalonate semialdehyde dehydrogenase deficiency genetic test at DNA Labs UAE is 4400 AED. This investment allows for a precise diagnosis, enabling healthcare providers to tailor treatment and management plans to the individual's genetic profile, potentially improving outcomes and quality of life for those affected by this rare metabolic disorder.
MMAB Gene Methylmalonic Aciduria CblB Type Genetic Test sale cost 4400 AED

MMAB Gene Methylmalonic Aciduria CblB Type Genetic Test Cost

The MMAB Gene Methylmalonic Aciduria CblB Type Genetic Test is a specialized diagnostic examination aimed at identifying mutations in the MMAB gene, which are associated with Methylmalonic Aciduria of the CblB type. This condition is an inherited disorder that disrupts the body's ability to process certain fats and proteins, leading to a buildup of methylmalonic acid in the blood. Symptoms can include vomiting, dehydration, developmental delays, and more severe neurological issues. The test is conducted by DNA Labs UAE, a leading facility in genetic diagnostics, ensuring high accuracy and reliability of results. With a cost of 4400 AED, the test is a critical tool for early detection and management of the disorder, allowing for tailored treatments and interventions that can significantly improve the quality of life for affected individuals and their families. By analyzing the patient's DNA for specific mutations in the MMAB gene, healthcare providers can confirm a diagnosis of Methylmalonic Aciduria CblB Type, facilitating appropriate genetic counseling and guiding treatment decisions.
MMACHC Gene Methylmalonic Aciduria CblC Type Genetic Test sale cost 4400 AED

MMACHC Gene Methylmalonic Aciduria CblC Type Genetic Test Cost

The MMACHC gene methylmalonic aciduria (cobalamin deficiency) cblC type genetic test is a specialized diagnostic tool used to identify mutations in the MMACHC gene, which are responsible for causing methylmalonic aciduria cblC type. This condition is an inherited metabolic disorder characterized by the body's inability to process certain fats and proteins properly, leading to a buildup of toxic substances like methylmalonic acid in the body. Symptoms can include developmental delay, feeding difficulties, lethargy, and failure to thrive, among others. Early detection through genetic testing can be crucial in managing symptoms and preventing serious complications. The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the MMACHC gene. By opting for this test at DNA Labs UAE, patients can expect comprehensive support, from initial consultation through to result interpretation and advice on management or treatment options. This test is a vital resource for families with a history of the condition or for individuals showing symptoms of methylmalonic aciduria cblC type, offering a pathway to better understanding and managing this genetic disorder.
MMADHC Gene Methylmalonic Aciduria CblD Type Genetic Test sale cost 4400 AED

MMADHC Gene Methylmalonic Aciduria CblD Type Genetic Test Cost

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.
LMBRD1 Gene Methylmalonic Aciduria CblF Type Genetic Test sale cost 4400 AED

LMBRD1 Gene Methylmalonic Aciduria CblF Type Genetic Test Cost

The LMBRD1 Gene Methylmalonic Aciduria CblF Type Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the LMBRD1 gene responsible for Methylmalonic Aciduria (MMA) CblF type. This condition is a rare metabolic disorder characterized by the body's inability to properly process certain fats and proteins, leading to a buildup of methylmalonic acid in the blood. The test is crucial for early detection and management of the disorder, potentially preventing severe metabolic crises and promoting better health outcomes. Performed through a detailed analysis of the patient's genetic material, this test specifically looks for alterations in the LMBRD1 gene, which are indicative of the CblF type of Methylmalonic Aciduria. Early diagnosis through this genetic testing can enable targeted treatment strategies, dietary management, and monitoring to mitigate the effects of the disorder. The cost of the LMBRD1 Gene Methylmalonic Aciduria CblF Type Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive evaluation necessary to confirm the presence of the genetic mutation, providing essential information for affected individuals and their families to manage the condition effectively.
ABCD4 Gene Methylmalonic Aciduria CblJ Type Genetic Test sale cost 4400 AED

ABCD4 Gene Methylmalonic Aciduria CblJ Type Genetic Test Cost

The "ABCD4 Gene Methylmalonic Aciduria CblJ Type Genetic Test" is a specialized diagnostic assessment aimed at identifying mutations in the ABCD4 gene, which are linked to a rare form of methylmalonic aciduria, known as cblJ type. Methylmalonic aciduria is a metabolic disorder that disrupts the body's ability to process certain fats and proteins, leading to a buildup of methylmalonic acid in the body. This can result in various health issues, including developmental delays, intellectual disabilities, and physical health problems. The test is specifically designed to detect genetic variations in the ABCD4 gene that are responsible for this condition, enabling healthcare providers to make an accurate diagnosis. Early detection through genetic testing can be crucial for managing symptoms, implementing dietary restrictions, and considering treatment options to improve the quality of life for affected individuals. This genetic test is available at DNA Labs UAE, a leading facility in the region for genetic testing and analysis. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the specialized expertise required to interpret the results. For families and individuals facing symptoms indicative of methylmalonic aciduria, this test offers a valuable tool for understanding their genetic health and making informed decisions about their care.
CD320 Gene Methylmalonic Aciduria CblR Type Genetic Test sale cost 3200 AED

CD320 Gene Methylmalonic Aciduria CblR Type Genetic Test Cost

The "CD320 Gene Methylmalonic Aciduria CblR Type Genetic Test" is a specialized diagnostic examination performed to identify mutations in the CD320 gene, which are linked to a rare genetic disorder known as Methylmalonic Aciduria (MMA) CblR type. This condition is characterized by the body's inability to properly process certain fats and proteins, leading to a buildup of methylmalonic acid in the blood. Symptoms can range from mild to severe and may include vomiting, dehydration, developmental delays, and more. The test is conducted through DNA Labs UAE, a leading facility in genetic and molecular diagnostics. By analyzing a patient's DNA sample, usually obtained from a blood draw, the test can pinpoint specific mutations in the CD320 gene that are responsible for this disorder. This information is crucial for confirming a diagnosis, understanding the severity of the condition, and guiding treatment and management strategies. The cost of the CD320 Gene Methylmalonic Aciduria CblR Type Genetic Test is 3200 AED. This price reflects the specialized nature of the test, which requires advanced technology and expertise to accurately identify the genetic mutations associated with the condition. Patients considering this test are advised to consult with a healthcare professional to discuss its benefits and implications for their health management plan.
MCEE Gene Methylmalonyl-CoA Epimerase Deficiency Genetic Test sale cost 4400 AED

MCEE Gene Methylmalonyl-CoA Epimerase Deficiency Genetic Test Cost

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.
MVK Gene Mevalonic Aciduria Genetic Test sale cost 4400 AED

MVK Gene Mevalonic Aciduria Genetic Test Cost

The MVK Gene Mevalonic Aciduria Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the MVK gene, which are known to cause Mevalonic Aciduria (MVA), a rare genetic disorder. This condition is part of the mevalonate kinase deficiency spectrum, which also includes Hyper-IgD Syndrome. Mevalonic Aciduria is characterized by a range of symptoms including developmental delay, recurrent fever, failure to thrive, and dysmorphic facial features, among others. The disorder results from a deficiency in mevalonate kinase, an enzyme crucial for cholesterol and isoprenoid biosynthesis. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in a laboratory setting. By examining the genetic makeup of the MVK gene, this test can confirm the presence of mutations that lead to the enzyme deficiency causing the disorder. Early diagnosis through genetic testing is vital for managing symptoms and improving the quality of life for affected individuals. The MVK Gene Mevalonic Aciduria Genetic Test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, which reflects the comprehensive analysis and detailed report provided by the lab. DNA Labs UAE employs state-of-the-art technology and adheres to international standards to ensure accurate and reliable results. This test is an essential tool for families seeking answers to unexplained symptoms that may be linked to genetic disorders, offering a pathway towards targeted treatment and management strategies.
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