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CLN3 Gene Ceroid lipofuscinosis neuronal type 3 Genetic Test Cost
The CLN3 gene ceroid lipofuscinosis neuronal type 3 genetic test is a specialized diagnostic tool used to identify mutations in the CLN3 gene, which are responsible for a rare, inherited neurodegenerative disorder known as Batten disease or juvenile neuronal ceroid lipofuscinosis (JNCL). This condition is characterized by progressive vision loss, cognitive impairment, and motor deficits, typically manifesting in childhood. The genetic test is crucial for confirming the diagnosis, enabling early intervention, and facilitating family planning decisions. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test costs 4400 AED. Through a sample of blood or saliva, DNA Labs UAE offers comprehensive analysis and interpretation of the CLN3 gene, aiming to provide patients and their families with essential information for managing the condition.
DNAJC5 Gene Ceroid lipofuscinosis neuronal type 4 Genetic Test Cost
The DNAJC5 gene is associated with a rare genetic disorder known as Ceroid Lipofuscinosis Neuronal Type 4 (CLN4), which is a form of Batten disease. This condition is characterized by an accumulation of lipopigments in the body's tissues, leading to progressive neurological impairment. Symptoms can include vision loss, motor dysfunction, seizures, and cognitive decline, typically manifesting in adulthood. A genetic test for the DNAJC5 gene helps in diagnosing CLN4, enabling early intervention and management of the condition. This test specifically looks for mutations in the DNAJC5 gene that are known to cause the disease. Early diagnosis can be crucial in managing symptoms and improving the quality of life for affected individuals. The test for the DNAJC5 gene linked to Ceroid Lipofuscinosis Neuronal Type 4 is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is 4400 AED. By opting for this test at DNA Labs UAE, patients and their families can expect accurate and reliable results, which are essential for planning appropriate treatment and care strategies for those diagnosed with CLN4.
PRF1 Gene Aplastic anemia Genetic Test Cost
The PRF1 Gene Aplastic Anemia Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the PRF1 gene, which are linked to the development of aplastic anemia. Aplastic anemia is a rare but serious condition characterized by the bone marrow's inability to produce sufficient new cells to replenish blood cells. The PRF1 gene plays a crucial role in the immune system, and mutations in this gene can lead to an increased risk of developing this condition. This test is particularly important for individuals with a family history of aplastic anemia or those who exhibit symptoms associated with the disease, such as fatigue, shortness of breath, irregular heart rate, pale skin, or frequent infections. Early detection through the PRF1 Gene Aplastic Anemia Genetic Test can facilitate timely intervention and management strategies to mitigate the impact of the condition. The test is conducted at DNA Labs UAE, a facility renowned for its state-of-the-art genetic testing services. The cost of the test is 4400 AED, reflecting the sophisticated nature of the technology and expertise required to accurately identify mutations in the PRF1 gene. Upon completion, the test provides individuals and their healthcare providers with critical information that can guide treatment decisions and, potentially, improve patient outcomes.
SBDS Gene Aplastic anemia SBDS related Genetic Test Cost
The SBDS gene plays a crucial role in the development and maintenance of the bone marrow, which is essential for producing healthy blood cells. Mutations in the SBDS gene can lead to a rare and serious condition known as Shwachman-Diamond Syndrome (SDS), which can manifest in various ways, including aplastic anemia. Aplastic anemia is a disorder where the bone marrow fails to produce sufficient amounts of blood cells, leading to a host of health issues including fatigue, higher risk of infections, and bleeding disorders. To diagnose or confirm a link between SBDS gene mutations and aplastic anemia, a genetic test can be conducted. In the UAE, DNA Labs offers a specialized test for this purpose. This test involves analyzing the patient's DNA to identify mutations in the SBDS gene that are associated with Shwachman-Diamond Syndrome and its related aplastic anemia. The cost of the SBDS gene-related genetic test at DNA Labs UAE is 4400 AED. This test is crucial for individuals who exhibit symptoms of aplastic anemia or have a family history of SDS, as it can provide a definitive diagnosis. A positive result can guide the treatment plan and also offers the possibility of genetic counseling for affected families, helping them understand the risks and implications for future offspring. It's important to note that such a test should be conducted under the guidance of a healthcare professional or genetic counselor, who can interpret the results accurately and offer the appropriate advice and support.
APOA2 Gene Apolipoprotein A-II deficiency Genetic Test Cost
The APOA2 gene is responsible for the production of Apolipoprotein A-II, a key component of high-density lipoprotein (HDL) in the bloodstream. This protein plays a crucial role in the regulation of lipid metabolism and the maintenance of cardiovascular health. A deficiency in Apolipoprotein A-II can lead to various metabolic disorders, including increased risk of coronary artery disease and other cardiovascular issues. To identify individuals at risk of Apolipoprotein A-II deficiency, a genetic test is available at DNA Labs UAE. This test examines the APOA2 gene for mutations that could lead to reduced levels or functionality of Apolipoprotein A-II. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed for specific genetic variations associated with the condition. The cost of the Apolipoprotein A-II deficiency genetic test at DNA Labs UAE is 4400 AED. This price includes the full analysis and a comprehensive report detailing the findings. The results of this test can provide valuable information for individuals concerned about their cardiovascular health, allowing them to take proactive steps in managing their risk factors in consultation with healthcare professionals.
HSD11B2 Gene Apparent mineralocorticoid excess Genetic Test Cost
The HSD11B2 gene test is a specialized genetic analysis aimed at diagnosing apparent mineralocorticoid excess (AME), a rare hereditary disorder. This condition arises due to mutations in the HSD11B2 gene, which plays a crucial role in the regulation of cortisol metabolism. Individuals with AME exhibit symptoms akin to those caused by an excess of mineralocorticoids, such as hypertension and low potassium levels, despite having normal mineralocorticoid levels. This is because the defective HSD11B2 gene leads to an inability to convert cortisol into its inactive form in certain tissues, mimicking the effects of excessive mineralocorticoid activity. DNA Labs UAE offers this genetic test for a cost of 4400 AED. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the lab to identify mutations in the HSD11B2 gene. The results can provide crucial information for the diagnosis and management of AME, guiding treatment decisions to manage symptoms effectively and reduce the risk of complications. This test is particularly valuable for individuals showing clinical signs of AME or those with a family history of the condition, enabling early intervention and personalized care.
ARG1 Gene Arginase deficiency Genetic Test Cost
The ARG1 Gene Arginase Deficiency Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the ARG1 gene that lead to arginase deficiency. This condition, also known as argininemia, is a rare but serious inherited disorder that affects the body's ability to properly break down arginine, an important amino acid. Without timely diagnosis and management, arginase deficiency can lead to severe neurological impairments, growth delays, and other health complications. The test involves analyzing the patient's DNA to pinpoint specific genetic mutations in the ARG1 gene, which are responsible for the enzyme arginase's malfunctioning. By identifying these mutations, healthcare providers can confirm a diagnosis of arginase deficiency, enabling them to tailor a treatment and management plan that addresses the unique needs of the patient. DNA Labs UAE offers this crucial genetic test for a cost of 4400 AED. The test is conducted in a state-of-the-art laboratory setting by a team of skilled geneticists and laboratory technicians, ensuring accurate and reliable results. For families and individuals facing symptoms suggestive of arginase deficiency, this test represents a vital step towards achieving a clearer understanding of the condition and securing the necessary interventions to improve health outcomes.
GATM Gene Arginine-glycine amidinotransferase deficiency Genetic Test Cost
The GATM gene, responsible for encoding the enzyme arginine-glycine amidinotransferase, plays a crucial role in the creatine biosynthesis pathway. Deficiencies in this enzyme can lead to a range of metabolic disorders, affecting muscle and brain function due to disrupted creatine production. To diagnose such deficiencies, a genetic test targeting the GATM gene can be performed. This test examines the DNA for mutations in the GATM gene that might lead to arginine-glycine amidinotransferase deficiency. DNA Labs UAE offers this specific genetic test, providing a valuable tool for diagnosing individuals who may be experiencing symptoms related to GATM gene deficiencies. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for any genetic abnormalities in the GATM gene. The cost of the GATM Gene Arginine-glycine amidinotransferase Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This price includes the full process of sample collection, genetic analysis, and the provision of results. Upon completion, a comprehensive report is provided, detailing any detected mutations and offering insights that can guide further medical consultation or intervention. This test is particularly important for individuals showing symptoms of creatine deficiency syndromes or for those with a family history of related metabolic disorders, as early detection can significantly impact management and treatment options.
