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SLC25A13 Gene Citrin deficiency Genetic Test Cost
The SLC25A13 gene is responsible for encoding a protein called citrin, which plays a crucial role in the urea cycle and the metabolism of amino acids and carbohydrates in the body. A deficiency in citrin caused by mutations in the SLC25A13 gene can lead to a range of metabolic disorders, including Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency (NICCD) and Citrullinemia Type II. These conditions can manifest with symptoms such as jaundice, failure to thrive, liver dysfunction, and in more severe cases, neurological issues. To diagnose citrin deficiency and related metabolic disorders accurately, genetic testing of the SLC25A13 gene is employed. This test involves analyzing the DNA to identify mutations in the SLC25A13 gene that are known to cause citrin deficiency. It is a crucial step in confirming the diagnosis, which can then guide appropriate management and treatment plans for affected individuals. In the UAE, DNA Labs offers the SLC25A13 gene citrin deficiency genetic test, providing a reliable diagnosis for those suspected of having this condition. The test cost is set at 4400 AED. By opting for this test at DNA Labs UAE, patients can expect a comprehensive analysis, ensuring accurate diagnosis and the potential for timely intervention to manage symptoms and improve quality of life.
ASS1 Gene Citrullinemia Genetic Test Cost
The ASS1 Gene Citrullinemia Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the ASS1 gene, which is pivotal for diagnosing Citrullinemia, a rare genetic disorder. Citrullinemia results from the body's inability to eliminate ammonia from the bloodstream due to a deficiency in the enzyme argininosuccinate synthetase, which is crucial for the urea cycle. This condition can lead to harmful levels of ammonia in the blood, causing severe implications for an individual's health, including neurological impairments and, if untreated, can be life-threatening. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, typically through a blood draw or a cheek swab, to analyze the genetic makeup of the ASS1 gene. This comprehensive analysis helps in identifying any mutations that may lead to the dysfunction of the enzyme responsible for ammonia detoxification in the liver. The cost of the ASS1 Gene Citrullinemia Genetic Test at DNA Labs UAE is set at 4400 AED. This price reflects the sophisticated technology and expertise required to accurately diagnose this condition, ensuring that individuals receive the necessary information for proper management and treatment. Early detection through this genetic test can significantly improve the quality of life for those affected by Citrullinemia by allowing for timely interventions and personalized treatment plans.
COQ6 Gene Coenzyme Q10 deficiency type 6 Genetic Test Cost
The COQ6 gene coenzyme Q10 deficiency type 6 genetic test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the COQ6 gene, which are associated with a rare form of coenzyme Q10 deficiency. This condition is a mitochondrial disorder that can affect multiple systems of the body, including the nervous system and the kidneys. Symptoms can vary widely among affected individuals but may include muscle weakness, seizures, developmental delays, and kidney failure. The test is crucial for the early detection and management of this condition, allowing for appropriate treatment strategies, including supplementation with coenzyme Q10 and other supportive therapies, to be implemented. This can significantly improve the quality of life for individuals with coenzyme Q10 deficiency type 6. The cost of the COQ6 gene coenzyme Q10 deficiency type 6 genetic test at DNA Labs UAE is 4400 AED. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect mutations in the COQ6 gene. The process is conducted by experienced professionals to ensure accurate and reliable results. Given the complexity and the specialized nature of the test, the cost reflects the extensive resources required for precise genetic analysis.
COQ4 Gene Coenzyme Q10 deficiency type 7 Genetic Test Cost
The COQ4 gene plays a crucial role in the biosynthesis of Coenzyme Q10 (CoQ10), a vital molecule for energy production and antioxidant protection within the body's cells. Mutations in the COQ4 gene can lead to Coenzyme Q10 deficiency type 7, a rare genetic condition that can affect multiple systems in the body, leading to symptoms such as muscle weakness, seizures, developmental delays, and in severe cases, heart failure. To diagnose this condition, genetic testing for the COQ4 gene mutation is available. DNA Labs UAE offers a specific test to identify mutations in the COQ4 gene, helping in the diagnosis of Coenzyme Q10 deficiency type 7. The test is crucial for confirming the diagnosis, understanding the disease's progression, and guiding treatment decisions, which may include CoQ10 supplementation and supportive therapies. The cost of the COQ4 Gene Coenzyme Q10 deficiency type 7 Genetic Test at DNA Labs UAE is 4400 AED. This test is a significant step towards personalized medicine, enabling affected individuals and their families to receive targeted interventions and manage the condition more effectively.
ABCB1 Gene Colchicine resistance Genetic Test Cost
The ABCB1 Gene Colchicine Resistance Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to evaluate an individual's genetic predisposition to resist the effects of colchicine, a medication commonly used for treating conditions such as gout and familial Mediterranean fever (FMF). The test focuses on identifying variations in the ABCB1 gene, which encodes a protein that plays a critical role in drug transport and metabolism. Certain mutations in the ABCB1 gene can affect how colchicine is processed in the body, leading to reduced efficacy of the drug. Understanding an individual's ABCB1 gene status can be crucial for healthcare providers to make informed decisions regarding colchicine dosing and exploring alternative treatments if necessary. This genetic test is particularly valuable for patients who have not responded to standard colchicine therapy, as it helps in tailoring a more effective and personalized treatment plan. DNA Labs UAE offers this genetic testing service at a cost of 4400 AED. The test involves a simple sample collection process, after which the sample is analyzed to detect any genetic variations associated with colchicine resistance. Results from the test provide comprehensive insights that can significantly impact the management of conditions for which colchicine is prescribed, ensuring patients receive the most appropriate and effective care based on their genetic makeup.
CLN5 Gene Ceroid lipofuscinosis neuronal type 5 Genetic Test Cost
The CLN5 gene ceroid lipofuscinosis neuronal type 5 genetic test is a specialized diagnostic tool designed to detect mutations in the CLN5 gene, which are linked to a rare inherited disorder known as neuronal ceroid lipofuscinosis type 5 (NCL5). This condition is part of a group of progressive neurodegenerative diseases that affect the nervous system, leading to symptoms such as vision loss, motor decline, and cognitive impairment. The test is crucial for early diagnosis, enabling timely intervention and management of the disease. Performed at DNA Labs UAE, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific genetic mutations associated with NCL5. The cost of the test is 4400 AED, reflecting the specialized nature of the analysis and the expertise required to accurately interpret the results. By identifying the presence of CLN5 mutations, the test provides essential information for families affected by this condition, facilitating genetic counseling and supporting decisions regarding treatment and care.
CLN6 Gene Ceroid lipofuscinosis neuronal type 6 Genetic Test Cost
The CLN6 gene ceroid lipofuscinosis neuronal type 6 genetic test is a specialized diagnostic tool used to identify mutations in the CLN6 gene, which are linked to a rare, inherited neurodegenerative disorder known as neuronal ceroid lipofuscinosis type 6 (NCL6). This condition is part of a group of disorders that lead to progressive deterioration of the nervous system, manifesting in symptoms such as vision loss, motor function decline, and cognitive impairment. Early and accurate diagnosis through genetic testing can be crucial for management and treatment planning. Performed at DNA Labs UAE, the test involves analyzing the patient's DNA to detect mutations in the CLN6 gene that are responsible for the condition. This state-of-the-art facility ensures accurate and reliable results, utilizing the latest in genetic testing technology. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed report provided to patients or their caregivers. By opting for this test, individuals suspected of having NCL6 can gain valuable insights into their condition, enabling healthcare providers to devise a tailored approach to treatment and management, potentially improving quality of life and outcomes.
BLM Gene Bloom syndrome Genetic Test Cost
The BLM Gene Bloom Syndrome Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to detect mutations in the BLM gene, which are indicative of Bloom syndrome. Bloom syndrome is a rare genetic disorder characterized by short stature, sun-sensitive skin changes, and an increased risk of developing various types of cancer at an early age. The condition is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected. This test is crucial for individuals with a family history of Bloom syndrome or those exhibiting symptoms, as early detection can lead to better management of the condition and its associated risks. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the BLM gene. At DNA Labs UAE, the BLM Gene Bloom Syndrome Genetic Test is priced at 4400 AED. This cost includes the full testing procedure and a comprehensive report of the findings. Given the complexity of genetic testing and the critical information it provides, this test is a valuable tool for individuals seeking to understand their genetic health and take proactive steps in managing their well-being.
