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SEC23B Gene Anemia Dyserythropoietic Type 2 Genetic Test Cost
The SEC23B Gene Anemia Dyserythropoietic Type 2 Genetic Test is a specialized diagnostic tool used to identify mutations in the SEC23B gene, which are associated with Congenital Dyserythropoietic Anemia Type II (CDA II). This condition is a rare, inherited blood disorder characterized by ineffective erythropoiesis, leading to anemia, jaundice, and an enlarged spleen. The test is crucial for confirming the diagnosis, understanding the disease's progression, and making informed decisions regarding management and treatment options. Performed at DNA Labs UAE, the test involves collecting a blood sample from the patient and analyzing the genetic material for specific mutations in the SEC23B gene. This state-of-the-art facility ensures accurate and reliable results, providing essential information for patients and their families. The cost of the SEC23B Gene Anemia Dyserythropoietic Type 2 Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of a precise diagnosis cannot be underestimated, as it opens the door to targeted treatment plans and genetic counseling for affected families, potentially improving the quality of life for individuals with this rare condition.
SERPINA1 Gene Antitrypsin-alpha-1 deficiency Genetic Test Cost
The SERPINA1 gene encodes alpha-1 antitrypsin (AAT), a protein that plays a crucial role in protecting the lungs from inflammation caused by infection or irritants like tobacco smoke. Mutations in the SERPINA1 gene can lead to alpha-1 antitrypsin deficiency (AATD), a genetic condition that significantly increases the risk of lung and liver diseases. AATD is often underdiagnosed but can have serious implications for affected individuals. To diagnose AATD, a genetic test is conducted, targeting the SERPINA1 gene to identify any mutations. This test is crucial for individuals with a family history of AATD or related pulmonary conditions, as early detection can lead to interventions that significantly improve quality of life and health outcomes. In the United Arab Emirates, DNA Labs UAE offers this specific genetic test for AATD. The cost of the test is 4400 AED. The test involves a simple blood draw or buccal swab, after which the sample is analyzed in the lab for the presence of mutations in the SERPINA1 gene. Results from this test can provide individuals with valuable information about their genetic predisposition to AATD and guide both patients and healthcare providers in managing and potentially mitigating the impact of the condition.
HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency Genetic Test Cost
The HMGCS2 gene encodes the enzyme 3-hydroxy-3-methylglutaryl-CoA synthase 2, which plays a crucial role in the process of ketogenesis. This metabolic pathway occurs in the liver, converting fatty acids into ketone bodies, which serve as an essential energy source during prolonged fasting or carbohydrate restriction. A deficiency in the HMGCS2 enzyme can disrupt this process, leading to a range of metabolic issues and clinical symptoms, including hypoglycemia, lethargy, and in severe cases, neurological impairment. To diagnose this condition, a genetic test targeting the HMGCS2 gene can be conducted. This test specifically looks for mutations in the HMGCS2 gene that could lead to enzyme deficiency. It is a critical tool for confirming the diagnosis, enabling appropriate management and treatment strategies for affected individuals. In the UAE, this specific genetic test is available at DNA Labs UAE, a leading facility in genetic diagnostics. The cost of the HMGCS2 Gene 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency Genetic Test is 4400 AED. This test is instrumental for families with a history of metabolic disorders or for individuals presenting symptoms suggestive of HMGCS2 deficiency. Early detection through this genetic testing allows for timely intervention, potentially mitigating the severity of the condition's impact on the patient's health.
HADH Gene 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Genetic Test Cost
The HADH Gene 3-Hydroxyacyl-CoA Dehydrogenase Deficiency Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at detecting mutations in the HADH gene. This gene plays a critical role in the metabolism of fatty acids within the body, and its mutations can lead to 3-Hydroxyacyl-CoA Dehydrogenase Deficiency. This condition can result in a variety of metabolic problems, ranging from hypoglycemia to more severe metabolic crises. Early detection through this genetic test is crucial for the management and treatment of the condition, helping to prevent potential complications. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the presence of HADH gene mutations. By choosing DNA Labs UAE for this testing, patients can expect reliable results, which are essential for the subsequent management of the condition. DNA Labs UAE is known for its state-of-the-art facilities and highly qualified staff, ensuring that the testing process is both efficient and effective.
HIBCH Gene 3-Hydroxyisobutryl-CoA Hydrolase Deficiency Genetic Test Cost
The "HIBCH Gene 3-Hydroxyisobutryl-CoA Hydrolase Deficiency Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the HIBCH gene. These mutations are associated with 3-Hydroxyisobutryl-CoA Hydrolase Deficiency, a rare metabolic disorder that can lead to various health issues, including developmental delay, neurological problems, and metabolic acidosis. The test is crucial for early diagnosis and management of the condition, enabling healthcare providers to devise appropriate treatment plans tailored to the patient's specific needs. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately identify the genetic anomaly responsible for the disorder.
MCCC1 Gene 3-Methylcrontonyl-CoA Carboxylase 1 Deficiency Genetic Test Cost
The MCCC1 gene plays a crucial role in the metabolism of certain proteins and fats within the body. A deficiency in 3-Methylcrotonyl-CoA Carboxylase 1, which is encoded by the MCCC1 gene, can lead to a metabolic disorder known as 3-Methylcrotonyl-CoA Carboxylase Deficiency. This condition can result in various health issues, including developmental delay, intellectual disability, and metabolic acidosis if not diagnosed and managed properly. To diagnose this condition, a genetic test can be conducted to identify mutations in the MCCC1 gene that are responsible for the deficiency. DNA Labs UAE offers this specific genetic test, providing a crucial tool for early detection and management of the condition. The test cost is set at 4400 AED, making it accessible for those in need of this specialized diagnostic service. Early detection through this genetic testing can lead to timely intervention, potentially mitigating some of the adverse effects associated with 3-Methylcrotonyl-CoA Carboxylase 1 Deficiency.
MCCC2 Gene 3-Methylcrontonyl-CoA Carboxylase 2 Deficiency Genetic Test Cost
The "MCCC2 Gene 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the MCCC2 gene. These mutations can lead to 3-Methylcrotonyl-CoA Carboxylase 2 deficiency, a rare metabolic disorder that affects the body's ability to process certain proteins properly. This condition can lead to various health issues, including developmental delay, metabolic acidosis, and in some cases, life-threatening complications if not diagnosed and managed early. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific genetic alterations associated with the disorder. The goal is to provide a definitive diagnosis, enabling targeted treatment and management plans to improve patient outcomes. The cost of the MCCC2 Gene 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the sophisticated genetic analysis required to detect the presence of mutations in the MCCC2 gene, offering peace of mind and critical health insights for affected individuals and their families.
AUH Gene 3-Methylglutaconic Aciduria Type 1 Genetic Test Cost
The AUH Gene 3-Methylglutaconic Aciduria Type 1 Genetic Test is a specialized diagnostic tool designed to detect mutations in the AUH gene, which are responsible for 3-Methylglutaconic Aciduria Type 1, a rare metabolic disorder. This condition is characterized by the body's inability to properly process certain proteins, leading to an accumulation of 3-methylglutaconic acid and related compounds in the body. Symptoms can vary but may include developmental delay, intellectual disability, and other neurological or physical issues. Performed at DNA Labs UAE, this genetic test involves analyzing the patient's DNA to identify mutations in the AUH gene that indicate the presence of 3-Methylglutaconic Aciduria Type 1. The test is critical for early diagnosis, which can aid in managing symptoms and improving the quality of life for affected individuals. The cost of the AUH Gene 3-Methylglutaconic Aciduria Type 1 Genetic Test is 4400 AED. This investment covers the sophisticated procedures required to accurately identify the genetic mutations associated with this condition. Given the complexity and the specialized nature of this test, it is conducted in the highly equipped and technologically advanced facilities of DNA Labs UAE, ensuring accurate and reliable results for patients and their families.