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FANCA Gene Fanconi anemia type A Genetic Test Cost
The FANCA Gene Fanconi Anemia Type A Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the FANCA gene, which is closely associated with Fanconi anemia type A. This condition is a rare genetic disorder that affects the bone marrow, leading to decreased production of all types of blood cells. People affected by this condition may also have physical abnormalities, an increased risk of certain cancers, and other serious health problems. The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. With a focus on accuracy and confidentiality, DNA Labs UAE provides comprehensive genetic testing services, including the FANCA gene test. This particular test is essential for individuals with a family history of Fanconi anemia or those showing symptoms of the disorder, as early detection can significantly impact the management and treatment of the condition. The cost of the FANCA Gene Fanconi Anemia Type A Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the intricate processes involved in genetic testing, from the extraction and analysis of DNA to the interpretation of results by genetic experts. Although the cost might seem high, the test provides invaluable information that can guide healthcare decisions, inform family planning, and potentially save lives through early intervention.
FANCB Gene Fanconi anemia type B Genetic Test Cost
The "FANCB Gene Fanconi Anemia Type B Genetic Test" is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the FANCB gene, which are responsible for Fanconi anemia type B. Fanconi anemia is a rare genetic disorder that leads to bone marrow failure and increased risk of cancer. The FANCB gene plays a crucial role in the body's ability to repair DNA damage, and mutations in this gene can disrupt this process, leading to the development of the disease. This test is particularly important for individuals with a family history of Fanconi anemia or those presenting symptoms related to the condition, such as physical abnormalities, bone marrow failure, or early onset of cancers. Early detection through the FANCB gene test can facilitate timely intervention and management of the disease, potentially improving the quality of life and survival rates of affected individuals. DNA Labs UAE offers this test at a cost of 4400 AED. The test involves collecting a DNA sample, typically through a blood draw, which is then analyzed in the laboratory for any mutations in the FANCB gene. Results from this test can provide crucial information for families regarding the risk of Fanconi anemia in current or future offspring and can guide decisions regarding genetic counseling and management strategies for the condition.
FANCC Gene Fanconi anemia type C Genetic Test Cost
The "FANCC Gene Fanconi Anemia Type C Genetic Test" is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the FANCC gene, which are associated with Fanconi anemia type C. Fanconi anemia is a rare, inherited blood disorder that leads to bone marrow failure and increased risk of cancer. The FANCC gene plays a crucial role in the DNA repair mechanism, and mutations in this gene can impair cellular functions, leading to the clinical manifestations of the disease. This genetic test is pivotal for individuals with a family history of Fanconi anemia or those exhibiting symptoms related to the disorder, as it can provide definitive confirmation of the condition. Early diagnosis through this test can significantly influence management and treatment strategies, potentially improving patient outcomes. The test is priced at 4400 AED and is conducted in the state-of-the-art facilities of DNA Labs UAE. The laboratory is equipped with the latest technology and staffed by experts in genetic diagnostics, ensuring accurate and reliable results. Individuals undergoing this test can expect a thorough analysis of the FANCC gene for any mutations indicative of Fanconi anemia type C.
FANCD2 Gene Fanconi anemia type D2 Genetic Test Cost
The FANCD2 Gene Fanconi Anemia type D2 Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the FANCD2 gene, which is crucial for diagnosing Fanconi Anemia (FA) type D2. Fanconi Anemia is a rare genetic disorder that affects the bone marrow, leading to decreased production of all types of blood cells. This condition can also predispose individuals to cancer and cause various congenital abnormalities. The FANCD2 gene plays a significant role in the FA pathway, a crucial DNA repair mechanism. Mutations in this gene can disrupt the pathway, leading to the characteristic symptoms and complications of FA. Early detection through genetic testing is vital for managing the disease effectively, as it allows for timely intervention and personalized treatment plans. This specific genetic test is available at DNA Labs UAE, a reputable facility known for its advanced diagnostic services. The test cost is set at 4400 AED, reflecting the intricate technology and expertise required to accurately identify mutations in the FANCD2 gene. By opting for this test at DNA Labs UAE, patients and their families can expect reliable results, which are essential for confirming the diagnosis of Fanconi Anemia type D2 and facilitating appropriate medical and genetic counseling.
FANCF Gene Fanconi anemia type F Genetic Test Cost
The FANCF Gene Fanconi Anemia Type F Genetic Test is a specialized diagnostic tool designed to identify mutations in the FANCF gene, which are indicative of Fanconi anemia type F. Fanconi anemia is a rare genetic disorder that leads to bone marrow failure and increased risk of cancer. The FANCF gene plays a crucial role in the body's ability to repair damaged DNA, and mutations in this gene can impair this process, leading to the development of the disease. This test is particularly valuable for individuals who have a family history of Fanconi anemia or present with symptoms suggestive of the condition, such as physical abnormalities, bone marrow failure, or certain cancers at a young age. Early diagnosis through genetic testing like the FANCF Gene Fanconi Anemia Type F Genetic Test can facilitate timely intervention and management strategies to address the complications associated with this condition. The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics, ensuring high standards of accuracy and reliability. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the FANCF gene. By opting for this test, individuals can gain crucial insights into their genetic health, empowering them with the information needed to make informed decisions about their medical care and that of their family members.
FANCG Gene Fanconi anemia type G Genetic Test Cost
The FANCG Gene Fanconi Anemia Type G Genetic Test is a specialized diagnostic procedure designed to identify mutations in the FANCG gene, which are implicated in the development of Fanconi anemia type G, a rare genetic disorder. This condition is part of a group of inherited diseases that affect the bone marrow, leading to decreased production of all types of blood cells. Fanconi anemia type G is characterized by physical abnormalities, bone marrow failure, and increased risk for certain types of cancer. The test involves analyzing the patient's DNA to look for specific mutations in the FANCG gene that are known to cause the disease. Early detection through this genetic testing is crucial for managing the condition effectively. It allows for appropriate interventions and monitoring for potential complications associated with Fanconi anemia, such as leukemia and other cancers. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the FANCG Gene Fanconi Anemia Type G Genetic Test is available for a cost of 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in genetic analysis, ensuring accurate and reliable test results. This test is essential for families with a history of Fanconi anemia, as it can help in making informed decisions regarding treatment options and genetic counseling.
CTNS Gene Cystinosis nephropathic Genetic Test Cost
The CTNS Gene Cystinosis Nephropathic Genetic Test is a specialized diagnostic procedure designed to identify mutations in the CTNS gene, which are responsible for causing nephropathic cystinosis. This condition is a rare, inherited metabolic disorder characterized by the accumulation of cystine within cells, leading to damage in various organs, especially the kidneys and eyes. Early diagnosis through genetic testing is crucial for managing the disease effectively and mitigating its progression. Performed at DNA Labs UAE, this test offers a comprehensive analysis of the CTNS gene to detect the specific genetic mutations associated with nephropathic cystinosis. The procedure involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory using advanced genetic sequencing technologies. The cost of the CTNS Gene Cystinosis Nephropathic Genetic Test is 4400 AED. This investment in health allows for an accurate diagnosis, enabling healthcare providers to tailor treatment plans to the individual's genetic profile, improving outcomes and quality of life for affected individuals.
CYP1A2 Gene Cytochrome P450 deficiency Genetic Test Cost
The CYP1A2 gene plays a critical role in the body's ability to process and eliminate various substances, including medications, caffeine, and environmental toxins. It encodes an enzyme belonging to the cytochrome P450 family, which is pivotal in the metabolism of drugs and other xenobiotics. Variations or deficiencies in the CYP1A2 gene can significantly impact an individual's response to certain medications, leading to adverse effects or reduced efficacy. To assess the functionality and identify any potential deficiencies in the CYP1A2 gene, a specialized genetic test is available. Conducted at DNA Labs UAE, this test is designed to provide insights into the genetic makeup of the individual regarding the CYP1A2 gene. It involves collecting a DNA sample, usually through a simple and non-invasive method such as a cheek swab or a blood sample, which is then analyzed to detect any variations that might affect the enzyme's activity. Understanding the results of this test can be crucial for personalized medicine, allowing healthcare providers to tailor drug therapies based on the patient's genetic predisposition. This can help in optimizing drug dosages, reducing the risk of adverse drug reactions, and improving overall treatment outcomes. The cost of the CYP1A2 Gene Cytochrome P450 deficiency genetic test at DNA Labs UAE is 4400 AED. Given the potential benefits in personalized healthcare and the prevention of adverse drug reactions, this test represents a valuable investment in an individual's health and well-being.
