Search Results for: results
ACADVL Gene Acyl-CoA Very Long-Chain Dehydrogenase Deficiency Genetic Test Cost
The ACADVL gene encodes for acyl-CoA dehydrogenase, an enzyme crucial for the breakdown of very long-chain fatty acids. A deficiency in this enzyme, known as Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD), can lead to serious metabolic problems, including hypoglycemia, liver dysfunction, and muscle weakness. It is a genetic condition that can manifest from infancy through adulthood, with varying degrees of severity. To diagnose VLCADD, a genetic test targeting the ACADVL gene can be performed. This test identifies mutations in the ACADVL gene that are responsible for the condition. It is a critical step not only for confirming the diagnosis but also for guiding treatment plans and understanding the risk of passing the condition to future generations. In the UAE, DNA Labs offers this specific genetic test for VLCADD. The cost of the test is 3200 AED. Conducting the test at DNA Labs UAE provides individuals and families with accurate, reliable results, leveraging advanced genetic testing technologies to ensure high-quality diagnostics. The test involves collecting a small sample of blood or saliva from the patient, which is then analyzed for mutations in the ACADVL gene. The process is straightforward, with results typically available within a few weeks, providing crucial information for managing and treating VLCADD effectively.
APRT Gene Adenine Phosphoribosyltransferase Deficiency Genetic Test Cost
The APRT Gene Adenine Phosphoribosyltransferase Deficiency Genetic Test is a specialized diagnostic tool used to detect deficiencies in the APRT gene, which can lead to a rare condition known as Adenine Phosphoribosyltransferase Deficiency. This condition affects the body's ability to break down adenine, leading to the accumulation of 2,8-dihydroxyadenine (2,8-DHA) crystals, which can cause kidney stones, kidney damage, or even kidney failure if left untreated. This genetic test involves analyzing the patient's DNA to identify mutations in the APRT gene that are responsible for the enzyme deficiency. Early detection through this test is crucial for managing symptoms, preventing complications, and improving the quality of life for affected individuals. The test is available at DNA Labs UAE, a leading facility known for its advanced genetic testing services. The cost of the APRT Gene Adenine Phosphoribosyltransferase Deficiency Genetic Test is set at 3200 AED. This price includes the full testing process, from sample collection to detailed analysis and reporting. Patients seeking this test can expect a comprehensive service that combines state-of-the-art technology with expert interpretation of results, ensuring accurate and reliable diagnoses.
ADSL Gene Adenylosuccinase Deficiency Genetic Test Cost
The ADSL Gene Adenylosuccinase Deficiency Genetic Test is a specialized diagnostic tool aimed at detecting mutations in the ADSL gene, which is responsible for adenylosuccinate lyase deficiency. This rare inherited disorder affects the metabolism of purines, essential building blocks of DNA and RNA, leading to a spectrum of neurological and physical symptoms ranging from mild to severe. Symptoms can include developmental delay, intellectual disability, epilepsy, and autistic behaviors, making early detection crucial for managing the condition. Performed at DNA Labs UAE, this genetic test involves analyzing the patient's DNA to identify any abnormalities or mutations in the ADSL gene that might indicate the presence of the deficiency. The process is meticulous and requires a sample of the patient's blood or saliva, which is then subjected to advanced genetic sequencing techniques to pinpoint the exact nature of the genetic anomaly. The cost of the ADSL Gene Adenylosuccinase Deficiency Genetic Test is set at 4400 AED. While this might seem significant, the price reflects the complex technology and expertise required to accurately diagnose this condition. Early diagnosis through this test can significantly impact the management of the disorder, allowing for tailored treatments and interventions that can improve the quality of life for affected individuals and their families.
CYP11B1 Gene Adrenal Hyperplasia Due to Steroid 11-Beta-Hydroxylase Deficiency Genetic Test Cost
The CYP11B1 gene plays a crucial role in the production of steroid hormones in the adrenal gland by encoding the enzyme 11-beta-hydroxylase. This enzyme is vital for the final steps of cortisol and aldosterone synthesis. Mutations in the CYP11B1 gene can lead to a condition known as congenital adrenal hyperplasia due to steroid 11-beta-hydroxylase deficiency. This genetic disorder disrupts the normal production of steroid hormones, leading to symptoms such as hypertension, low potassium levels, and in severe cases, ambiguous genitalia in females. To diagnose this condition, a genetic test targeting the CYP11B1 gene mutations can be conducted. This test is crucial for confirming the diagnosis, understanding the condition's severity, and guiding treatment options. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the test is 4400 AED. Conducting the test at DNA Labs UAE ensures that individuals receive accurate and reliable results, benefiting from the lab's expertise in genetic diagnostics and state-of-the-art technology. This test is an essential tool for affected families to make informed decisions regarding the management and treatment of this condition.
NR0B1 Gene Adrenal Hypoplasia Genetic Test Cost
The NR0B1 gene adrenal hypoplasia genetic test is a diagnostic procedure aimed at identifying mutations in the NR0B1 gene, which are linked to adrenal hypoplasia congenita (AHC), a rare condition that affects adrenal gland development. This condition can lead to a critical deficiency in the production of adrenal hormones, which are crucial for regulating metabolism, the immune system, and blood pressure. The NR0B1 gene plays a significant role in the development and function of the adrenal glands and reproductive system. Mutations in this gene can lead to various health issues, including adrenal insufficiency and hypogonadotropic hypogonadism. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific mutations in the NR0B1 gene. The results can provide valuable information for the diagnosis, management, and treatment planning of individuals with or at risk of developing AHC. Additionally, it can be crucial for family planning decisions for affected families. The cost of the NR0B1 gene adrenal hypoplasia genetic test at DNA Labs UAE is 4400 AED. This cost reflects the specialized nature of the test, the advanced technology used in the analysis, and the professional expertise required to interpret the results accurately.
ATIC Gene AICA-Ribosiduria Due to ATIC Deficiency Genetic Test Cost
The "ATIC Gene AICA-Ribosiduria Due to ATIC Deficiency Genetic Test" is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the ATIC gene, which can lead to AICA-ribosiduria. This rare genetic disorder is characterized by an accumulation of AICA-riboside in bodily fluids and is caused by a deficiency in the ATIC enzyme, which plays a critical role in the purine biosynthesis pathway. Symptoms of the disorder may include developmental delay, physical disabilities, and neurological issues. This test is crucial for individuals who exhibit symptoms suggestive of AICA-ribosiduria or have a family history of the disorder, as early detection can aid in managing symptoms and improving the quality of life. The testing process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed for specific mutations in the ATIC gene that are known to cause the condition. The cost of the ATIC Gene AICA-Ribosiduria Due to ATIC Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to accurately identify the presence of the genetic mutation, providing essential information for diagnosis and potential treatment options. Given the specialized nature of this test and its importance in the diagnosis of a rare genetic disorder, the cost reflects the technical expertise and resources necessary to conduct the analysis and interpret the results.
HGD Gene Alkaptonuria Genetic Test Cost
The HGD Gene Alkaptonuria Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the HGD gene, which is responsible for alkaptonuria. Alkaptonuria is a rare inherited disorder that causes the body to be unable to properly break down certain amino acids, leading to a buildup of homogentisic acid in the body. This can result in darkening of the urine, arthritis, heart disease, and other complications. The test is crucial for early detection and management of the condition, allowing for interventions that can significantly improve the quality of life for those affected. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the HGD gene that are known to cause alkaptonuria. At DNA Labs UAE, the cost for the HGD Gene Alkaptonuria Genetic Test is set at 4400 AED. This price includes the full testing process, from sample collection to the comprehensive analysis and final report detailing the findings. It's important for individuals with a family history of alkaptonuria or those experiencing symptoms to consider this test, as early detection is key to managing the disease effectively.
A2M Gene Alpha-2-Macroglobulin Deficiency Genetic Test Cost
The A2M Gene Alpha-2-Macroglobulin Deficiency Genetic Test is a specialized diagnostic procedure designed to detect mutations in the A2M gene, which can lead to Alpha-2-Macroglobulin (A2M) deficiency. This condition is characterized by a lack of A2M, a vital plasma protein that plays a crucial role in the body's immune response and in protecting tissues from enzymes that could damage them. Identifying mutations in the A2M gene is essential for understanding the risk of developing related conditions, such as chronic obstructive pulmonary disease (COPD), liver cirrhosis, and certain types of cancer. Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers individuals the opportunity to gain insights into their genetic makeup, particularly concerning the A2M gene. The test is performed using a blood sample, from which DNA is extracted and analyzed for any abnormalities in the A2M gene. The cost of the A2M Gene Alpha-2-Macroglobulin Deficiency Genetic Test is 4400 AED. This price reflects the comprehensive nature of the test, including the advanced technology and expertise required to accurately identify mutations in the A2M gene. For individuals with a family history of conditions associated with A2M deficiency or those experiencing symptoms related to these conditions, this test provides a valuable tool for early detection and management, potentially improving health outcomes and quality of life.
