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CA5A Gene Hyperammonemia Due to Carbonic Anhydrase VA Deficiency Genetic Test Cost
The CA5A gene hyperammonemia due to carbonic anhydrase VA deficiency genetic test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to detect mutations in the CA5A gene. These mutations can lead to a rare metabolic disorder characterized by an inability to properly process and eliminate ammonia from the body, resulting in hyperammonemia. This condition, known as carbonic anhydrase VA deficiency, can cause a variety of symptoms, ranging from mild to severe, including neurological impairment and developmental delays. The test is conducted through a detailed analysis of the patient's DNA, aiming to identify any genetic abnormalities in the CA5A gene that could disrupt the function of carbonic anhydrase VA, an enzyme critical for ammonia detoxification and energy production. Early detection through this genetic test is crucial, as it can lead to timely intervention and management of the condition, potentially preventing serious complications. At DNA Labs UAE, the cost for this comprehensive genetic test is set at 4400 AED. The facility ensures accurate and reliable results, utilizing state-of-the-art genetic testing technologies and adhering to stringent quality control measures. Patients undergoing this test at DNA Labs UAE can expect a professional service, with support and guidance provided throughout the testing process, from sample collection to the interpretation of results.
CYP24A1 Gene Hypercalcemia Infantile Type Genetic Test Cost
The "CYP24A1 Gene Hypercalcemia Infantile Type Genetic Test" is a specialized diagnostic tool designed to identify mutations in the CYP24A1 gene, which are known to cause infantile hypercalcemia. This condition is characterized by abnormally high levels of calcium in the blood during infancy, which can lead to various health complications if left untreated. The test is crucial for early detection, enabling timely intervention and management strategies to mitigate potential health issues associated with the condition. Performed at DNA Labs UAE, the test involves analyzing the patient's DNA to look for specific genetic mutations in the CYP24A1 gene. These mutations disrupt the normal breakdown of vitamin D, leading to increased calcium absorption and hypercalcemia. Identifying these mutations can help in confirming the diagnosis, understanding the severity of the condition, and guiding treatment decisions. The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the expertise required to interpret the results accurately. Given the implications of early detection on the patient's health outcomes, the test represents a critical investment in the health and well-being of infants suspected of having this genetic condition.
CA12 Gene Hyperchlorhidrosis Isolated Genetic Test Cost
The "CA12 Gene Hyperchlorhidrosis Isolated Genetic Test" is a specialized genetic analysis designed to detect mutations in the CA12 gene, which are associated with hyperchlorhidrosis. Hyperchlorhidrosis is a condition characterized by excessive sweating beyond what is typically required for body temperature regulation. This test is particularly valuable for individuals experiencing severe sweating without clear environmental or physiological causes, as it can confirm a genetic predisposition to this condition. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample from the patient, usually through a blood draw or a cheek swab. The sample is then analyzed to identify any genetic variations in the CA12 gene that may contribute to hyperchlorhidrosis. The cost of the CA12 Gene Hyperchlorhidrosis Isolated Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test and the sophisticated technology and expertise required to accurately identify mutations in the CA12 gene. Patients considering this test should consult with a healthcare provider or a genetic counselor to discuss its implications, potential results, and the course of action based on the test outcomes.
BAAT Gene Hypercholanemia Genetic Test Cost
The BAAT Gene Hypercholanemia Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, aimed at identifying mutations in the BAAT gene, which are linked to hypercholanemia—a condition characterized by an abnormal increase in bile acid levels in the blood. This condition can lead to various gastrointestinal issues and liver diseases. By analyzing a patient's DNA, the test can determine the presence of genetic alterations in the BAAT gene, providing essential information for the diagnosis, management, and treatment planning of hypercholanemia. The test is priced at 4400 AED, making it an accessible option for individuals in the UAE seeking comprehensive genetic analysis for this specific condition.
TJP2 Gene Hypercholanemia Genetic Test Cost
The TJP2 Gene Hypercholanemia Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the TJP2 gene, which are known to cause hypercholanemia—a condition characterized by elevated levels of bile acids in the blood. This condition can lead to various liver problems, including jaundice, itching, and potentially more severe liver damage over time. Early detection through genetic testing is crucial for managing symptoms and preventing complications. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or a cheek swab. The sample is then analyzed to detect any genetic variations in the TJP2 gene that might predispose individuals to hypercholanemia. This test is particularly recommended for individuals with a family history of liver disease or those exhibiting symptoms related to elevated bile acids. The cost of the TJP2 Gene Hypercholanemia Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test, the expertise required to accurately interpret the results, and the advanced technology utilized in the testing process. Given the potential health implications of hypercholanemia, this test represents a valuable investment in one's health, providing crucial information for the management and treatment of this condition.
LDLRAP1 Gene Hypercholesterolemia Autosomal Recessive Genetic Test Cost
The LDLRAP1 gene plays a crucial role in regulating cholesterol levels within the body. Mutations in this gene can lead to a condition known as autosomal recessive hypercholesterolemia, characterized by elevated levels of low-density lipoprotein (LDL) cholesterol in the blood. This condition increases the risk of developing early cardiovascular diseases. To diagnose this genetic predisposition, a specific genetic test targeting the LDLRAP1 gene is available. Conducted at DNA Labs UAE, this test is designed to detect mutations in the LDLRAP1 gene that are responsible for the autosomal recessive form of hypercholesterolemia. By analyzing a patient's DNA, the test can confirm the presence of these genetic variations, providing essential information for early diagnosis and management of the condition. The cost of the LDLRAP1 gene hypercholesterolemia autosomal recessive genetic test is 4400 AED. This investment can be crucial for individuals with a family history of hypercholesterolemia, enabling them and their healthcare providers to take proactive steps in managing their cholesterol levels and reducing the risk of heart disease.
COG7 Gene Glycosylation Disorder Type 2E Genetic Test Cost
The COG7 Gene Glycosylation Disorder Type 2E Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the COG7 gene, which are implicated in Congenital Disorders of Glycosylation Type IIe (CDG-IIe). This condition is a rare genetic disorder that affects the normal process of glycosylation - the attachment of sugars to proteins and lipids, which is crucial for various cellular functions. Symptoms of the disorder can include developmental delay, neurological issues, and abnormalities in various organs. The test, priced at 4400 AED, involves analyzing the patient's DNA to detect mutations in the COG7 gene, helping in the accurate diagnosis of CDG-IIe. This information is vital for understanding the prognosis of the disorder and can guide treatment and management strategies. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, the test ensures accuracy and reliability, providing essential genetic insights for affected individuals and their families.
SLC35A1 Gene Glycosylation Disorder Type 2F Genetic Test Cost
The SLC35A1 gene glycosylation disorder type 2F genetic test is a specialized diagnostic procedure aimed at identifying mutations in the SLC35A1 gene, which are associated with Congenital Disorders of Glycosylation (CDG). Type 2F CDG, a rare genetic condition, affects the body's ability to properly glycosylate proteins and lipids, which are crucial for various cellular functions. Symptoms of the disorder can vary widely among individuals but often include developmental delay, neurological issues, and problems with the digestive system, among others. Performed at DNA Labs UAE, this test is essential for confirming a diagnosis of SLC35A1-CDG and facilitating appropriate management and treatment plans for affected individuals. The test involves collecting a DNA sample, typically through a blood draw, and analyzing it for specific genetic alterations in the SLC35A1 gene that are indicative of the disorder. The cost of the SLC35A1 gene glycosylation disorder type 2F genetic test at DNA Labs UAE is 4400 AED. This price reflects the specialized nature of the test, the expertise required to accurately interpret the results, and the potential impact this diagnosis can have on patient care. For families and individuals facing symptoms suggestive of a congenital disorder of glycosylation, this test provides a critical step towards understanding their condition and navigating the complexities of genetic disorders.
