The Gastrointestinal Cancer Gene Panel Test is a sophisticated diagnostic tool designed to identify specific genetic mutations associated with various types of gastrointestinal cancers, including cancers of the stomach, colon, rectum, esophagus, and pancreas. By analyzing a patient's DNA, this comprehensive test can detect alterations in multiple genes that are known to increase the risk of developing gastrointestinal cancers.
Performed at DNA Labs UAE, a leading facility in genetic testing, the test offers a proactive approach for individuals with a family history of gastrointestinal cancers or those who want to assess their genetic predisposition to these diseases. The test cost is set at 7200 AED, reflecting the extensive analysis and detailed insights it provides. Results from this test can guide personalized prevention strategies, inform treatment decisions, and help in the early detection of cancers, significantly impacting patient outcomes.
The Glycogen Storage Disorder (GSD) Gene Panel Test is a comprehensive diagnostic tool offered by DNA Labs UAE, designed to detect genetic mutations associated with various types of Glycogen Storage Disorders. GSDs are a group of inherited metabolic conditions that affect the body's ability to store and release glucose from glycogen, leading to a range of symptoms from mild to severe, including muscle weakness, liver dysfunction, and in some cases, life-threatening complications.
This gene panel test specifically targets the genes known to be associated with the different forms of GSD, making it an essential step in confirming a diagnosis, understanding the specific type of GSD, and guiding treatment strategies. The test involves analyzing the patient's DNA to identify mutations in the genes related to glycogen storage and metabolism.
At DNA Labs UAE, the Glycogen Storage Disorder Gene Panel Test is priced at 7200 AED. The test process is streamlined and conducted by experienced professionals, ensuring accuracy and reliability in the results. Once the test is completed, genetic counselors at DNA Labs UAE can provide valuable insights into the implications of the test results, potential treatments, and management strategies for individuals diagnosed with a Glycogen Storage Disorder.
The Haemophilia A and B Gene Panel Test is a comprehensive diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the genes responsible for haemophilia A and B. Haemophilia A, also known as classic haemophilia, is primarily caused by mutations in the F8 gene, leading to a deficiency in clotting factor VIII. Haemophilia B, on the other hand, results from mutations in the F9 gene, which causes a deficiency in clotting factor IX. Both conditions are inherited in an X-linked recessive pattern, predominantly affecting males.
This gene panel test is a crucial step in diagnosing these bleeding disorders, enabling healthcare providers to make informed decisions regarding treatment plans and management strategies. It involves analyzing the patient's DNA to identify any genetic mutations associated with haemophilia A and B, offering a high degree of accuracy and specificity.
Priced at 7200 AED, the test is conducted in the state-of-the-art facilities of DNA Labs UAE, ensuring quality and reliability. The cost reflects the comprehensive nature of the test, covering a detailed analysis that can guide patient care and inform family planning decisions for those affected by or carriers of haemophilia. By opting for this test, patients and their families gain valuable insights into their genetic makeup, empowering them with information crucial for managing the condition effectively.
The Hemochromatosis HFE Full Gene Sequence Analysis Test is a comprehensive genetic screening designed to detect mutations in the HFE gene, which are commonly associated with hereditary hemochromatosis. Hereditary hemochromatosis is a genetic disorder that causes the body to absorb an excessive amount of iron from the diet, leading to iron overload in various organs and tissues. If left untreated, this condition can result in significant health issues, including liver disease, heart problems, diabetes, and arthritis.
The test involves analyzing the entire gene sequence of HFE to identify mutations that may predispose an individual to developing hemochromatosis. This level of analysis can provide valuable information for individuals with a family history of the condition or those exhibiting symptoms related to iron overload.
Performed at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, the Hemochromatosis HFE Full Gene Sequence Analysis Test is priced at 7200 AED. The cost reflects the comprehensive nature of the test, employing cutting-edge technology to ensure accurate and reliable results. By opting for this test, individuals can gain insights into their genetic risk for hemochromatosis, enabling them to take proactive steps in managing their health in consultation with healthcare professionals.
Leigh Syndrome, also known as Mitochondrial Encephalopathy, is a severe neurological disorder that typically arises in the first year of life. This condition is characterized by progressive loss of mental and movement abilities, which can lead to severe neurological and physical impairment. Leigh Syndrome is caused by genetic mutations affecting the mitochondria, the energy-producing structures within cells, leading to energy production failure and, subsequently, cell death, particularly in the brain, muscles, and heart.
To diagnose this complex condition, a Mitochondrial Encephalopathy Gene Panel Test is utilized. This comprehensive genetic test screens for mutations in multiple genes known to be associated with Leigh Syndrome and other mitochondrial disorders. By examining a broad panel of genes, this test provides a more accurate diagnosis, guiding treatment options and management strategies for affected individuals.
The test is available at DNA Labs UAE, a leading facility in genetic testing and diagnostics. The cost of the Mitochondrial Encephalopathy Gene Panel Test is 7200 AED. Conducting the test in a specialized and reputable laboratory like DNA Labs UAE ensures high accuracy and reliability of the results, which is crucial for the effective management of Leigh Syndrome and related mitochondrial disorders. This test is a critical step in the journey towards understanding and managing these complex conditions, offering hope for affected families through precise diagnosis and the potential for targeted therapies.
The Lysosomal Storage Disorder (LSD) Gene Panel Test is a comprehensive genetic screening designed to identify mutations in genes associated with lysosomal storage disorders, a group of rare inherited metabolic conditions. This panel test is crucial for the early diagnosis and management of these disorders, enabling healthcare providers to tailor treatment plans effectively. By analyzing a wide range of genes linked to various forms of LSDs, the test offers a detailed insight into the genetic underpinnings of these conditions, which can include Gaucher disease, Fabry disease, Pompe disease, and many others.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability in results, thanks to their state-of-the-art technology and expert team. The cost of the Lysosomal Storage Disorder Gene Panel Test is set at 7200 AED, reflecting the comprehensive nature of the analysis and the significant value it provides in guiding patient care and genetic counseling. This test is a vital tool for individuals with a family history of lysosomal storage disorders or presenting symptoms suggestive of these conditions, offering a path towards a clearer understanding of their health and proactive management options.
The Metabolic Disorder Gene Panel Test, available at DNA Labs UAE, is a comprehensive diagnostic tool designed to identify genetic mutations associated with a wide range of metabolic disorders. Priced at 7200 AED, this advanced genetic test offers a deep insight into the genetic factors that may contribute to metabolic issues, allowing for precise diagnosis, informed treatment decisions, and personalized management plans. By examining specific genes known to affect metabolism, the test can uncover genetic predispositions to conditions such as lipid metabolism disorders, mitochondrial disorders, and various inborn errors of metabolism. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test is a crucial step towards proactive health management and tailored healthcare, providing individuals and families with critical information to address metabolic disorders effectively.
The Microcephaly Gene Panel Test is a specialized genetic test designed to identify mutations in genes associated with microcephaly, a condition characterized by a smaller head size than that typical for an infant's age and sex. This condition can result from a variety of genetic factors and can lead to developmental delays and neurological problems. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient's DNA to pinpoint specific genetic mutations linked to microcephaly. The comprehensive nature of this panel test makes it a crucial tool for diagnosing the condition accurately, thereby facilitating appropriate medical and developmental interventions. The cost of the Microcephaly Gene Panel Test at DNA Labs UAE is 7200 AED, reflecting the intricate technology and expertise required to perform this advanced genetic analysis.
The Nervous System Cancer Gene Panel Test is a sophisticated diagnostic tool designed to identify genetic mutations associated with cancers of the nervous system. Conducted at DNA Labs UAE, this test screens for a comprehensive range of genetic markers that are known to influence the risk, development, and progression of nervous system cancers, including brain tumors. By analyzing a patient's DNA sample, usually obtained through a simple blood draw or biopsy, the test aims to provide critical insights into the genetic underpinnings of an individual's cancer, guiding personalized treatment strategies and management plans.
The cost of the Nervous System Cancer Gene Panel Test at DNA Labs UAE is 7200 AED. This investment covers the extensive analysis required to detect and interpret the specific genetic alterations that could impact a patient's cancer treatment and prognosis. The results from this test can help healthcare providers make informed decisions about targeted therapies, surveillance strategies, and potential participation in clinical trials, ultimately aiming to improve patient outcomes in the challenging landscape of nervous system cancers.
The Neuronal Ceroid Lipofuscinosis (NCL) Gene Panel Test is a comprehensive genetic test designed to identify mutations in genes associated with Neuronal Ceroid Lipofuscinosis, a group of progressive neurodegenerative disorders primarily affecting children. These disorders are characterized by the accumulation of lipofuscin, a fatty substance, in the body's tissues, leading to symptoms such as vision loss, motor decline, and seizures. The test analyzes multiple genes known to be linked to various forms of NCL, providing crucial information for accurate diagnosis and guiding treatment options.
Offered at DNA Labs UAE, this advanced genetic test is priced at 7200 AED. The facility utilizes cutting-edge technology and adheres to strict quality standards to ensure the reliability and accuracy of the test results. By opting for the NCL Gene Panel Test at DNA Labs UAE, patients and their families can gain valuable insights into the specific genetic mutations causing the disorder, facilitating early intervention and personalized care plans to manage the condition more effectively.
