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FAH Gene Tyrosinemia type 1 Genetic Test Cost
The FAH Gene Tyrosinemia Type 1 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the FAH gene, which are responsible for Tyrosinemia type 1. Tyrosinemia type 1 is a rare genetic disorder that affects the body's ability to metabolize the amino acid tyrosine, leading to liver disease, kidney problems, and neurological issues if left untreated. Early detection through this genetic test can be crucial for initiating timely treatment strategies, such as dietary management and medication, to prevent severe complications. DNA Labs UAE offers this test at a cost of 4400 AED. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for the presence of specific mutations in the FAH gene. Results from this test can provide valuable information for affected individuals and their families regarding the management of Tyrosinemia type 1, including considerations for genetic counseling and potential treatment plans.
GSTZ1 Gene Tyrosinemia type 1B Genetic Test Cost
The "GSTZ1 Gene Tyrosinemia Type 1B Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the GSTZ1 gene, which are linked to Tyrosinemia type 1B, a rare genetic disorder. This condition affects the body's ability to properly break down the amino acid tyrosine, leading to various health issues, including liver and kidney problems. The test is crucial for early detection and management of the disorder, enabling healthcare providers to tailor appropriate treatment plans for affected individuals. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify the genetic variations associated with Tyrosinemia type 1B.
PDP1 Gene Pyruvate Dehydrogenase Phosphatase Deficiency Genetic Test Cost
The PDP1 gene pyruvate dehydrogenase phosphatase deficiency genetic test is a specialized diagnostic procedure designed to identify mutations in the PDP1 gene. These mutations can lead to a rare metabolic disorder known as pyruvate dehydrogenase phosphatase deficiency. This condition affects the body's ability to convert carbohydrates into energy, leading to a range of symptoms including developmental delay, neurological issues, and lactic acidosis. The test is conducted by analyzing the patient's DNA to detect any genetic abnormalities in the PDP1 gene that may be causing the disorder. Early detection through this genetic testing is crucial for managing symptoms and improving the quality of life for affected individuals. This specific test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, which reflects the comprehensive analysis and the specialized technology required to accurately identify mutations in the PDP1 gene. By choosing DNA Labs UAE for this test, patients can expect reliable results that can aid in the diagnosis and treatment planning for pyruvate dehydrogenase phosphatase deficiency.
PKLR Gene Pyruvate Kinase Deficiency with Hemolytic Anemia Genetic Test Cost
The PKLR gene plays a crucial role in the body's energy production process by encoding for the enzyme pyruvate kinase, which is essential in the glycolytic pathway. A mutation in this gene can lead to Pyruvate Kinase Deficiency, a rare genetic disorder that affects red blood cells, leading to hemolytic anemia. This condition is characterized by the premature destruction of red blood cells, resulting in symptoms such as fatigue, jaundice, an enlarged spleen, and increased susceptibility to infections. To diagnose this condition, a genetic test can be performed to identify mutations in the PKLR gene. This test is particularly vital for individuals showing symptoms of hemolytic anemia or those with a family history of the condition, as it can provide a definitive diagnosis and help in managing the disease effectively. In the UAE, DNA Labs offers this genetic test for PKLR gene mutations. The cost of the test is 4400 AED. Conducting the test at a reputable facility like DNA Labs UAE ensures accuracy and reliability of the results, which is crucial for the subsequent management and treatment of Pyruvate Kinase Deficiency. This test is a step forward in personalized medicine, offering affected individuals and their families the necessary information to understand their condition better and make informed health decisions.
PEX7 Gene Refsum Disease Genetic Test Cost
The PEX7 Gene Refsum Disease Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at identifying mutations in the PEX7 gene, which are responsible for the development of Refsum Disease. This rare genetic disorder affects the metabolism of phytanic acid, leading to its accumulation in the body and resulting in a variety of symptoms including vision and hearing loss, muscle weakness, and coordination problems. Early diagnosis through genetic testing can be crucial for managing the condition effectively. The test cost is set at 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify the genetic variations associated with this condition. Conducted in the state-of-the-art facilities of DNA Labs UAE, this test offers individuals and families critical insights into their genetic health, enabling informed decisions and personalized management plans for those affected by Refsum Disease.
PHYH Gene Refsum Disease Genetic Test Cost
The PHYH Gene Refsum Disease Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to detect mutations in the PHYH gene, which are indicative of Refsum Disease. This rare genetic disorder disrupts the normal breakdown of phytanic acid, a type of fatty acid found in the diet, leading to its accumulation in the body. The accumulation can cause a variety of symptoms, including vision and hearing loss, impaired coordination, and muscle weakness. The test, priced at 4400 AED, involves analyzing the patient's DNA to identify any genetic variations in the PHYH gene that are known to cause the condition. Early detection through this genetic testing is crucial for managing symptoms and preventing the progression of the disease. DNA Labs UAE provides this service with the aim of offering precise diagnostics to facilitate targeted interventions for individuals at risk of or suspected to have Refsum Disease.
SLC52A1 Gene Riboflavin Deficiency Genetic Test Cost
The SLC52A1 gene plays a crucial role in the body's metabolism of riboflavin (vitamin B2), an essential nutrient that supports energy production and cellular function. Mutations in the SLC52A1 gene can lead to riboflavin deficiency, which may result in a range of health issues, including neurological symptoms, growth retardation, and anemia. To identify individuals at risk of riboflavin deficiency due to genetic mutations, the SLC52A1 Gene Riboflavin Deficiency Genetic Test is available. This genetic test is a specialized diagnostic tool designed to detect mutations in the SLC52A1 gene. By analyzing a patient's DNA, the test can identify specific genetic variations that are known to impair riboflavin metabolism, helping healthcare providers to diagnose riboflavin deficiency accurately and tailor treatment plans accordingly. Such treatments may include dietary adjustments and riboflavin supplementation. The test is conducted at DNA Labs UAE, a leading facility known for its advanced genetic testing services. The cost of the SLC52A1 Gene Riboflavin Deficiency Genetic Test is 4400 AED. This investment allows individuals to gain valuable insights into their genetic predisposition to riboflavin deficiency, enabling early intervention and personalized nutritional strategies to mitigate the risk of associated health issues.
RPIA Gene Ribose 5-Phosphate Isomerase Deficiency Genetic Test Cost
The "RPIA Gene Ribose 5-Phosphate Isomerase Deficiency Genetic Test" is a specialized diagnostic procedure aimed at identifying mutations in the RPIA gene, which can lead to Ribose 5-Phosphate Isomerase Deficiency. This rare genetic disorder impacts the body's ability to properly metabolize carbohydrates, leading to a range of health issues including developmental delays, neurological problems, and other systemic complications. The test involves analyzing the patient's DNA to look for specific genetic alterations associated with the condition, providing crucial information for diagnosis, management, and treatment planning. Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the cost of the test is 4400 AED. This investment in health allows for a comprehensive understanding of the genetic underpinnings of the disorder, enabling targeted interventions and support for affected individuals and their families.