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AIFM1 Gene Combined oxidative phosphorylation deficiency type 6 Genetic Test Cost
The AIFM1 gene plays a crucial role in the process of oxidative phosphorylation, a critical pathway for energy production within cells. Mutations in the AIFM1 gene can lead to Combined Oxidative Phosphorylation Deficiency Type 6 (COXPD6), a rare genetic disorder that affects multiple body systems and can result in a wide range of symptoms, including muscle weakness, neurological deficits, and developmental delays. To diagnose this condition, genetic testing is available at DNA Labs UAE. The test specifically looks for mutations in the AIFM1 gene that are associated with COXPD6. It is a crucial step for affected individuals and their families to understand the underlying genetic cause of the condition, which can inform treatment decisions and help in assessing the risk for future children. The cost of the AIFM1 gene test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the presence of mutations in the AIFM1 gene. Given the complexity of genetic testing and the significant information it provides, the test is a valuable tool for individuals and families dealing with the implications of COXPD6.
C12ORF65 Gene Combined oxidative phosphorylation deficiency type 7 Genetic Test Cost
The C12ORF65 gene plays a critical role in the proper functioning of the mitochondrial translation machinery, which is essential for the synthesis of proteins involved in oxidative phosphorylation. Mutations in this gene can lead to Combined Oxidative Phosphorylation Deficiency Type 7 (COXPD7), a rare genetic disorder characterized by a wide range of symptoms, including muscle weakness, neurological deficits, and developmental delays, among others. Early and accurate diagnosis of COXPD7 is crucial for managing the symptoms and improving the quality of life of affected individuals. DNA Labs UAE offers a genetic test specifically designed to identify mutations in the C12ORF65 gene, aiding in the diagnosis of COXPD7. The test is conducted using a sample of the patient's DNA, usually obtained through a blood draw or a cheek swab. The procedure involves analyzing the genetic material for specific mutations known to be associated with the condition. The cost of the C12ORF65 gene test at DNA Labs UAE is 4400 AED. This comprehensive test is a critical tool for healthcare providers in diagnosing Combined Oxidative Phosphorylation Deficiency Type 7, allowing for timely intervention and management strategies tailored to the individual's specific needs. By offering this test, DNA Labs UAE contributes to the enhanced understanding and treatment of rare genetic disorders, supporting patients and their families in navigating these challenging conditions.
ALG11 Gene Congenital disorder of glycosylation type Ip Genetic Test Cost
The ALG11 gene plays a critical role in the process of glycosylation, which is the attachment of sugars to proteins and lipids, a critical process necessary for proper cellular function. Mutations in the ALG11 gene can lead to a rare condition known as Congenital Disorder of Glycosylation Type Ip (CDG-Ip), a genetic disorder that affects multiple systems of the body, including the nervous system, liver, and coagulation processes, leading to a wide range of potential symptoms such as developmental delay, liver dysfunction, and coagulation abnormalities. To diagnose this condition, a specific genetic test targeting the ALG11 gene can be conducted. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic testing service. The test is designed to identify mutations in the ALG11 gene that are responsible for CDG-Ip, providing essential information for accurate diagnosis and management of the disorder. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the comprehensive information it provides to healthcare providers, patients, and their families. Conducting this test at DNA Labs UAE involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory using advanced genetic sequencing technologies to detect mutations in the ALG11 gene. The results of this test can confirm a diagnosis of CDG-Ip, guide treatment decisions, and provide important information for genetic counseling of affected families.
CPOX Gene Coproporphyria Genetic Test Cost
The CPOX Gene Coproporphyria Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the CPOX gene. These mutations are responsible for a condition known as Hereditary Coproporphyria (HCP), a rare type of porphyria that affects the body's ability to produce heme, an essential component of hemoglobin. HCP is characterized by a range of symptoms including abdominal pain, neuropathy, and, in severe cases, neurological complications. The test, priced at 4400 AED, involves analyzing the patient's DNA to detect specific genetic alterations in the CPOX gene, enabling precise diagnosis and facilitating appropriate management and treatment strategies for affected individuals. By identifying the genetic basis of the condition, this test plays a crucial role in the clinical approach to managing Hereditary Coproporphyria, offering hope for better outcomes through personalized medicine.
LPA Gene Coronary artery disease susceptibility to Genetic Test Cost
The "LPA Gene Coronary Artery Disease Susceptibility Genetic Test" is a cutting-edge diagnostic tool available at DNA Labs UAE, designed to assess an individual's genetic predisposition to developing coronary artery disease (CAD). This test specifically examines variations in the LPA gene, which have been linked to an increased risk of CAD. The LPA gene encodes for a protein called lipoprotein(a), high levels of which in the blood can lead to the development of plaques in the arteries, thereby increasing the risk of heart attacks and other cardiovascular diseases. By analyzing a person's DNA, the test identifies specific mutations or polymorphisms within the LPA gene that are associated with elevated lipoprotein(a) levels and, consequently, a higher risk of coronary artery disease. This information can be invaluable for individuals with a family history of CAD or those who have other risk factors for the disease. The test is conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services. The cost of the LPA Gene Coronary Artery Disease Susceptibility Genetic Test is 4400 AED. The results from this test can provide individuals with critical insights into their genetic risk for CAD, allowing them to take proactive measures in consultation with healthcare professionals to mitigate this risk through lifestyle changes, medication, or other interventions deemed necessary based on the test findings and overall health assessment.
VKORC1 Gene Coumarin resistance Genetic Test Cost
The VKORC1 Gene Coumarin Resistance Genetic Test is a specialized diagnostic tool used to identify variations in the VKORC1 gene that can affect an individual's response to coumarin-based anticoagulants, such as warfarin. These medications are commonly prescribed to prevent blood clots, but their effectiveness and safety are highly dependent on precise dosing, which can vary significantly among individuals due to genetic differences. The VKORC1 gene plays a crucial role in the vitamin K cycle, which is essential for blood clotting, and mutations in this gene can lead to either increased sensitivity or resistance to coumarin drugs, necessitating adjustments to standard dosing to avoid complications such as bleeding or thrombosis. The test is conducted at DNA Labs UAE, a leading facility in genetic testing and personalized medicine. The cost of the test is 4400 AED, which reflects the comprehensive analysis and professional interpretation that accompany the genetic screening. By opting for this test, patients and healthcare providers can make more informed decisions regarding the use of coumarin-based anticoagulants, leading to safer and more effective treatment outcomes for conditions that require blood-thinning medication.
CYP2C9 Gene CoumarinWarfarin resistance due to CYP2C9 variants Genetic Test Cost
The CYP2C9 gene plays a crucial role in drug metabolism, particularly in the processing of Coumarin and Warfarin, commonly used anticoagulants. Variants in the CYP2C9 gene can significantly affect an individual's response to these medications, leading to resistance or increased sensitivity, which can impact treatment efficacy and safety. The genetic test for CYP2C9 variants is a valuable tool in personalized medicine, allowing healthcare providers to tailor anticoagulant dosages more accurately to the patient's genetic makeup. At DNA Labs UAE, the test for identifying CYP2C9 variants related to Coumarin/Warfarin resistance is available. This test is crucial for patients who are starting or currently on Coumarin or Warfarin therapy, as it helps in determining the most effective dosage and minimizing the risk of adverse drug reactions. The cost of the test is 4400 AED, which is an investment in ensuring safer and more effective treatment outcomes for patients requiring anticoagulant therapy. By understanding a patient's genetic predisposition to Coumarin/Warfarin resistance, healthcare providers can make informed decisions, potentially reducing the risk of bleeding or thrombotic events associated with improper dosing.
CR1 Gene CR1 deficiency Genetic Test Cost
The CR1 gene, also known as Complement Receptor 1, plays a crucial role in the immune system by helping to regulate the complement system, which is a part of the immune system that enhances the ability of antibodies and phagocytic cells to clear pathogens from an organism. A deficiency in the CR1 gene can lead to various immune system disorders and may increase susceptibility to infections and certain autoimmune diseases. To diagnose CR1 deficiency and understand its implications for an individual's health, a genetic test can be conducted. This test examines the CR1 gene for mutations that could lead to a deficiency in its function. It is a critical tool for individuals experiencing symptoms that may be linked to CR1 deficiency or for those with a family history of related immune system disorders. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the CR1 gene deficiency genetic test is 4400 AED. Conducted in a state-of-the-art laboratory by experienced geneticists and healthcare professionals, this test provides valuable insights into an individual's genetic makeup, specifically concerning the CR1 gene. The results can help guide treatment plans, preventive measures, and provide a better understanding of potential health risks related to CR1 deficiency.
