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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.
BCAT1 Gene Branched-chain aminotransferase 1 deficiency Genetic Test Cost
The BCAT1 Gene Branched-chain aminotransferase 1 deficiency genetic test is a specialized diagnostic assessment available at DNA Labs UAE. This test is designed to identify deficiencies in the BCAT1 gene, which is crucial for the metabolism of branched-chain amino acids (BCAAs) like leucine, isoleucine, and valine. These amino acids are essential for protein synthesis and energy production in various tissues, including muscle and brain. A deficiency in the BCAT1 gene can lead to metabolic imbalances and a range of health issues, including neurological disorders and delayed development. The test is conducted through a comprehensive analysis of the patient's DNA to detect mutations or anomalies in the BCAT1 gene. It is a vital tool for clinicians to diagnose the condition accurately, allowing for personalized treatment plans to manage symptoms and improve the quality of life for affected individuals. The cost of the BCAT1 Gene Branched-chain aminotransferase 1 deficiency genetic test at DNA Labs UAE is 4400 AED. This investment covers the detailed laboratory analysis required to ensure accurate and reliable results, offering invaluable insights into the patient's genetic health.
BCAT2 Gene Branched-chain aminotransferase 2 deficiency Genetic Test Cost
The BCAT2 gene is responsible for encoding the enzyme branched-chain aminotransferase 2, which plays a crucial role in the metabolism of branched-chain amino acids (BCAAs) like leucine, isoleucine, and valine. These amino acids are essential for protein synthesis and energy production in various tissues, including muscle and the brain. Deficiencies or mutations in the BCAT2 gene can lead to metabolic disorders, affecting the body's ability to process these vital nutrients properly. Genetic testing for BCAT2 gene deficiency is a precise method to diagnose potential metabolic issues linked to this gene. The test involves analyzing the individual's DNA to identify mutations in the BCAT2 gene that could lead to enzyme deficiencies or dysfunctions. Early detection through genetic testing is crucial as it allows for the implementation of dietary modifications and treatments to manage or mitigate the effects of the disorder. In the United Arab Emirates, DNA Labs UAE offers the BCAT2 Gene Branched-chain aminotransferase 2 Deficiency Genetic Test. The test is priced at 4400 AED and is conducted in their state-of-the-art facilities. DNA Labs UAE employs advanced genetic testing technologies to ensure accurate and reliable results, providing essential information for the management of conditions related to BCAT2 gene deficiencies. This test is an invaluable resource for individuals experiencing symptoms of metabolic disorders or those with a family history of such conditions, aiming to offer peace of mind and a path towards appropriate care and management.
BCKDK Gene Branched-chain ketoacid dehydrogenase kinase deficiency Genetic Test Cost
The BCKDK (Branched-Chain Ketoacid Dehydrogenase Kinase) gene plays a crucial role in the metabolism of branched-chain amino acids, which are essential nutrients obtained from proteins found in food. Mutations in the BCKDK gene can lead to a deficiency in the enzyme branched-chain ketoacid dehydrogenase kinase. This deficiency disrupts the normal breakdown of amino acids, leading to various metabolic problems and potentially severe neurological issues. To diagnose this condition, a genetic test is available at DNA Labs UAE, which specifically looks for mutations in the BCKDK gene. This test is vital for individuals showing symptoms of the deficiency or for those with a family history of metabolic disorders. Early diagnosis can help in managing the condition effectively through dietary modifications and, in some cases, supplementation. The cost of the BCKDK gene test at DNA Labs UAE is 4400 AED. The test is conducted using a sample of the patient's blood or saliva, and it involves analyzing the genetic material for specific mutations associated with the deficiency. The process is highly accurate and provides essential information for the diagnosis and management of the condition.
SCNN1A Gene Bronchiectasis with or without elevated sweat chloride type 2 Genetic Test Cost
The SCNN1A gene plays a crucial role in regulating the movement of sodium in and out of cells, particularly in the lungs and sweat glands. Mutations in this gene can lead to a condition known as Bronchiectasis with or without elevated sweat chloride type 2, a rare form of lung disease characterized by chronic inflammation and infection of the bronchi, leading to their dilatation. This condition can also affect sweat chloride levels, a marker typically used for diagnosing cystic fibrosis, although it presents differently. To diagnose this specific genetic condition, DNA Labs UAE offers a specialized genetic test targeting the SCNN1A gene. The test, priced at 4400 AED, involves analyzing the patient's DNA to identify mutations in the SCNN1A gene that are known to cause Bronchiectasis with or without elevated sweat chloride type 2. This precise genetic testing is crucial for accurate diagnosis, guiding treatment options, and understanding the risk of passing the condition on to offspring. DNA Labs UAE utilizes advanced genetic testing techniques to ensure reliable and accurate results for patients and their families.
BCHE Gene Butyrylcholinesterase deficiency Genetic Test Cost
The BCHE gene butyrylcholinesterase deficiency genetic test is a specialized diagnostic procedure aimed at identifying mutations in the BCHE gene, which is responsible for producing the enzyme butyrylcholinesterase (BChE). This enzyme plays a crucial role in the process of breaking down certain types of drugs and toxins in the body, including muscle relaxants used during surgical procedures. A deficiency in BChE can lead to prolonged paralysis or apnea after exposure to these substances, posing significant health risks during medical treatments. The test is particularly recommended for individuals with a family history of BChE deficiency, those who have experienced unexpected reactions to anesthesia, or for those who are planning to undergo surgery and wish to ensure safe anesthesia use. By analyzing a DNA sample, usually obtained from a blood draw, the test identifies specific genetic mutations in the BCHE gene that lead to reduced activity or absence of the butyrylcholinesterase enzyme. Conducted at DNA Labs UAE, a leading provider of genetic testing services, the test offers a comprehensive analysis with a focus on accuracy and confidentiality. The cost of the test is set at 4400 AED, reflecting the specialized nature of the testing and the expertise required to accurately interpret the results. Upon completion, the results can provide valuable information for patients and healthcare providers to make informed decisions regarding anesthesia use and to take precautions to mitigate potential risks associated with BChE deficiency.