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TFR2 Gene Hemochromatosis Type 3 Genetic Test Cost
The TFR2 Gene Hemochromatosis Type 3 Genetic Test is a specific diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the TFR2 gene, which are responsible for causing Type 3 Hemochromatosis. This condition, also known as Transferrin Receptor 2 Hemochromatosis, is a hereditary disorder characterized by excessive iron accumulation in the body, leading to various health issues such as liver disease, diabetes, and heart problems. The test is crucial for individuals with a family history of the condition or those exhibiting symptoms related to iron overload, as early detection can significantly improve management and treatment outcomes. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and detailed genetic insights it provides, aiding in the precise diagnosis and guiding appropriate therapeutic interventions.
SLC40A1 Gene Hemochromatosis Type 4 Genetic Test Cost
The SLC40A1 gene hemochromatosis type 4 genetic test is a specialized diagnostic procedure designed to identify mutations in the SLC40A1 gene, which are linked to a rare form of hereditary hemochromatosis, known as type 4 or ferroportin disease. This condition affects the body's ability to regulate iron absorption, leading to iron overload and potential damage to organs such as the liver, heart, and pancreas. Early detection through genetic testing is crucial for managing the condition effectively and preventing severe complications. The test involves collecting a DNA sample, usually through a blood draw, which is then analyzed in a laboratory setting to detect specific genetic mutations in the SLC40A1 gene. The outcome of this test can provide valuable information for individuals with a family history of the condition or those exhibiting symptoms related to iron overload, aiding in the diagnosis and guiding treatment decisions. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, the cost of the SLC40A1 gene hemochromatosis type 4 genetic test is set at 4400 AED. The test is performed by qualified professionals who ensure accuracy and confidentiality of the results, providing patients and their families with essential insights into their genetic health and risk factors related to hereditary hemochromatosis type 4.
G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test Cost
The G6PD Gene Hemolytic Anemia Due to G6PD Deficiency Genetic Test is a diagnostic procedure aimed at identifying individuals with Glucose-6-Phosphate Dehydrogenase (G6PD) deficiency, a genetic condition that can lead to hemolytic anemia. This condition arises when the body lacks enough G6PD enzyme, which is crucial for the normal processing of red blood cells. Without sufficient G6PD, red blood cells can be destroyed prematurely, leading to anemia. This test specifically searches for mutations in the G6PD gene, which are indicative of the deficiency. It's a vital tool for diagnosing individuals who exhibit symptoms of G6PD deficiency or those who are at risk due to their family history. Symptoms can range from fatigue and jaundice to severe cases of anemia triggered by infections, certain foods, or medications. Conducted at DNA Labs UAE, the test is priced at 4400 AED. The process involves collecting a blood sample from the individual, which is then analyzed in the laboratory for genetic markers of G6PD deficiency. The results of this test can provide crucial information for managing the condition, including guidance on avoiding certain triggers and insights into the risk of passing the deficiency on to offspring. This genetic test is a cornerstone in the proactive management of G6PD deficiency, offering individuals and their families the means to better understand and navigate this genetic condition.
GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test Cost
**GPI Gene Hemolytic Anemia Nonspherocytic Due to Glucose Phosphate Isomerase Deficiency Genetic Test** This specialized genetic test is conducted to diagnose a rare, inherited disorder known as Non-Spherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase (GPI) Deficiency. This condition affects the red blood cells, leading to their premature destruction (hemolysis) and resulting in various degrees of anemia, which is not characterized by the typical spherical shape of the cells seen in other forms of hemolytic anemia. The GPI enzyme plays a crucial role in the glycolytic pathway, and its deficiency can lead to inadequate energy production in red blood cells, causing them to be more susceptible to rupture. The test specifically looks for mutations in the GPI gene, which are responsible for this enzyme deficiency. Identifying mutations in the GPI gene can confirm the diagnosis and help in understanding the disease's severity, guiding treatment decisions, and providing information for genetic counseling. **Test Details:** - **Cost:** The test is priced at 4400 AED. - **Location:** The testing is available at DNA Labs UAE, a facility equipped with advanced genetic testing technology to ensure accurate and reliable results. - **Procedure:** It typically involves collecting a blood sample from the patient, which is then analyzed in the lab for any genetic abnormalities in the GPI gene. - **Duration:** The time frame from sample collection to receiving results may vary, so it is advisable to consult with DNA Labs UAE for specific details. This test is essential for individuals with a family history of GPI deficiency or those exhibiting symptoms of non-spherocytic hemolytic anemia, as early diagnosis can significantly improve management and outcome.
F8 Gene Hemophilia A Genetic Test Cost
The F8 Gene Hemophilia A Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the F8 gene, which are responsible for Hemophilia A, a genetic disorder that impairs the body's ability to make blood clots. This condition leads to excessive bleeding following an injury or surgery and can cause spontaneous bleeding episodes, particularly in the muscles and joints. Hemophilia A is inherited in an X-linked recessive pattern, affecting mainly males, while females can be carriers of the condition. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, the test involves collecting a blood sample from the patient. The sample is then analyzed to detect any abnormalities or mutations in the F8 gene that would indicate the presence of Hemophilia A. This test is crucial for the accurate diagnosis of Hemophilia A, enabling healthcare providers to devise appropriate management and treatment plans for affected individuals. The cost of the F8 Gene Hemophilia A Genetic Test at DNA Labs UAE is 4400 AED. This investment in genetic testing can be invaluable for families with a history of Hemophilia A, offering them insights into their genetic makeup and helping to manage or mitigate the effects of this disorder. Early diagnosis through genetic testing can significantly improve the quality of life for individuals with Hemophilia A by allowing for timely interventions and personalized care strategies.
HLCS Gene Holocarboxylase Synthetase Deficiency Genetic Test Cost
**HLCS Gene Holocarboxylase Synthetase Deficiency Genetic Test at DNA Labs UAE** The HLCS gene holocarboxylase synthetase deficiency genetic test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at identifying mutations in the HLCS gene. These mutations are responsible for a rare inherited metabolic disorder known as holocarboxylase synthetase deficiency. This condition affects the body's ability to break down certain proteins and carbohydrates, leading to a range of health issues that can be severe if not diagnosed and treated early. The test involves analyzing the patient's DNA to look for specific genetic alterations in the HLCS gene, which encodes an enzyme critical for biotin (vitamin B7) metabolism. Early diagnosis through this genetic testing allows for timely intervention, including dietary management and biotin supplementation, which can significantly improve outcomes and quality of life for affected individuals. DNA Labs UAE offers this comprehensive genetic testing service for a cost of 4400 AED. The test is conducted in a state-of-the-art facility by experienced geneticists and laboratory technicians, ensuring accurate and reliable results. Families with a history of metabolic disorders or individuals showing symptoms related to biotin deficiency are encouraged to consider this test for a definitive diagnosis and appropriate management of the condition.
IDUA Gene Hurler Syndrome Genetic Test Cost
The IDUA Gene Hurler Syndrome Genetic Test is a specialized diagnostic assessment performed to identify mutations in the IDUA gene, which are associated with Hurler Syndrome, a rare and severe form of mucopolysaccharidosis (MPS I). This condition is characterized by a deficiency of the enzyme alpha-L-iduronidase, leading to the accumulation of glycosaminoglycans in various body tissues, affecting physical appearance, organ function, and overall development. Early detection through genetic testing is crucial for managing symptoms, improving quality of life, and exploring treatment options, including enzyme replacement therapy and hematopoietic stem cell transplantation. The test is conducted at DNA Labs UAE, a state-of-the-art facility known for its comprehensive genetic testing services. The cost of the IDUA Gene Hurler Syndrome Genetic Test is 4400 AED. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the IDUA gene. The results of this test can provide valuable information for families affected by Hurler Syndrome, including the confirmation of a diagnosis, the identification of carriers within the family, and the guidance of future family planning decisions.
IDUA Gene Hurler-Scheie Syndrome Genetic Test Cost
The IDUA Gene Hurler-Scheie Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the IDUA gene, which are indicative of Hurler-Scheie syndrome. Hurler-Scheie syndrome is a rare genetic disorder that falls within the spectrum of mucopolysaccharidosis type I (MPS I), characterized by a wide range of symptoms from physical deformities to cognitive impairment, depending on the severity of the disease. The test is crucial for early diagnosis, enabling timely intervention and management of the condition. Priced at 4400 AED, this genetic test involves analyzing the patient's DNA to identify any abnormalities in the IDUA gene, which is responsible for producing the enzyme alpha-L-iduronidase. Deficiency in this enzyme leads to the accumulation of glycosaminoglycans, causing the various symptoms associated with the syndrome. The result from this test can provide essential information for families regarding treatment options, potential for disease progression, and genetic counseling.
