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SLC6A19 Gene Hartnup Disorder Genetic Test Cost
The SLC6A19 gene Hartnup disorder genetic test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the SLC6A19 gene, which are linked to Hartnup disorder. Hartnup disorder is a rare, inherited metabolic condition characterized by the body's inability to properly absorb and metabolize certain amino acids, leading to a variety of symptoms including skin rashes, neurological issues, and digestive problems. The test involves analyzing the patient's DNA to detect specific genetic alterations associated with the condition, providing crucial information for accurate diagnosis and management. DNA Labs UAE, a leading provider of genetic testing services in the region, conducts this test with precision and care, ensuring reliable results. The cost of the SLC6A19 gene Hartnup disorder genetic test is set at 4400 AED, reflecting the sophisticated technology and expertise required to perform this advanced diagnostic procedure. By opting for this test, individuals suspected of having Hartnup disorder or those with a family history of the condition can gain valuable insights into their genetic makeup, facilitating timely and appropriate interventions to manage symptoms and improve quality of life.
HFE Gene Hemochromatosis Classical Genetic Test Cost
The HFE Gene Hemochromatosis Classical Genetic Test is a critical diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the HFE gene, which are primarily responsible for hereditary hemochromatosis. This condition leads to excessive iron absorption by the body, potentially resulting in severe organ damage if left untreated. By analyzing a patient's DNA, this test can confirm the presence of common mutations such as C282Y and H63D, among others, associated with the disorder. Priced at 3200 AED, the test provides a crucial step towards the early detection and management of hereditary hemochromatosis, enabling patients to take proactive measures against the complications associated with this genetic condition.
PMM2 Gene Glycosylation Disorder Type 1A Genetic Test Cost
The PMM2 Gene Glycosylation Disorder Type 1A Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the PMM2 gene, which are associated with Congenital Disorders of Glycosylation Type 1a (CDG-Ia). CDG-Ia is a rare genetic condition that affects the normal process of adding sugar chains to proteins (glycosylation), which is crucial for various cellular functions. Symptoms of CDG-Ia can include developmental delay, neurological issues, and digestive problems, among others. This genetic test involves analyzing the patient's DNA to identify any mutations in the PMM2 gene that could lead to the disorder. The test is crucial for early diagnosis and management of the condition, allowing for appropriate treatment plans and interventions to be established. At DNA Labs UAE, the test is priced at 4400 AED, reflecting the comprehensive analysis and expertise required to accurately diagnose this complex genetic disorder.
MPI Gene Glycosylation Disorder Type 1B Genetic Test Cost
The "MPI Gene Glycosylation Disorder Type 1B Genetic Test" is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the MPI gene. These mutations are responsible for a rare condition known as Congenital Disorders of Glycosylation Type 1b (CDG-1b), which affects the body's ability to properly glycosylate proteins and lipids, essential processes for normal cellular function. CDG-1b can lead to a wide range of symptoms, including developmental delay, gastrointestinal problems, and liver dysfunction, among others. Given the complexity of this disorder and its potential impact on various body systems, early and accurate diagnosis is crucial for managing symptoms and improving quality of life. The test involves analyzing the patient's DNA to look for specific mutations in the MPI gene that are indicative of CDG-1b. This genetic testing is a critical step in confirming the diagnosis, enabling targeted treatment plans, and providing genetic counseling for affected families. The cost of the MPI Gene Glycosylation Disorder Type 1B Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the sophisticated nature of the testing process, which requires advanced genetic sequencing technologies and expert analysis to ensure accurate results. Patients and healthcare providers considering this test can expect a high level of diagnostic accuracy, which is essential for the effective management of CDG-1b.
ALG3 Gene Glycosylation Disorder Type 1D Genetic Test Cost
The ALG3 Gene Glycosylation Disorder Type 1D Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, aimed at identifying mutations in the ALG3 gene, which are associated with Congenital Disorders of Glycosylation (CDG). CDG Type 1D is a rare genetic condition that impacts the normal process of glycosylation, the addition of sugar chains to proteins, which is crucial for various cellular functions. Symptoms of the disorder can range from mild to severe, including developmental delay, intellectual disabilities, seizures, and problems with liver function. Priced at 4400 AED, the test involves analyzing the patient's DNA to detect any abnormalities in the ALG3 gene. Early detection through this genetic testing allows for better management of the condition, including tailored treatments and interventions that can significantly improve the quality of life for affected individuals. DNA Labs UAE utilizes advanced genetic testing technologies to ensure accurate and reliable results, providing essential information for families and healthcare providers managing this complex disorder.
MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test Cost
The MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test is a specialized diagnostic tool used to identify mutations in the MPDU1 gene, which can lead to a rare condition known as Congenital Disorder of Glycosylation Type 1F (CDG-1F). CDG-1F is a genetic disorder that affects the normal process of glycosylation, an essential biological mechanism where sugar molecules are attached to proteins and lipids, impacting various bodily functions. This specific test targets the MPDU1 gene to detect abnormalities that disrupt normal glycosylation processes, leading to a range of symptoms such as developmental delay, neurological issues, and abnormalities in liver function among others. Given the complexity and rarity of the condition, the test provides crucial information for accurate diagnosis, which is vital for managing symptoms and improving the quality of life for affected individuals. The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the MPDU1 Gene Glycosylation Disorder Type 1F Genetic Test is 4400 AED. This price reflects the sophisticated nature of the testing process, which involves advanced genetic sequencing techniques to accurately identify mutations in the MPDU1 gene. By opting for this test at DNA Labs UAE, patients and healthcare providers can expect reliable results, which are essential for the effective management and treatment of CDG-1F.
ALG8 Gene Glycosylation Disorder Type 1H Genetic Test Cost
The "ALG8 Gene Glycosylation Disorder Type 1H Genetic Test" is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the ALG8 gene, which are responsible for a rare condition known as Congenital Disorders of Glycosylation Type 1H (CDG-1H). This genetic disorder affects the body's ability to properly glycosylate proteins and lipids, which are crucial for various cellular functions. Symptoms of CDG-1H can vary widely among individuals but often include developmental delay, neurological issues, and digestive problems. The test is priced at 4400 AED and involves analyzing the patient's DNA to identify any abnormalities in the ALG8 gene that may lead to the disorder. The process is meticulous and requires a blood sample from the patient. DNA Labs UAE employs cutting-edge genetic sequencing technologies to ensure accurate and reliable results. This test is critical for early diagnosis and management of the condition, potentially improving the quality of life for affected individuals and their families. It also offers valuable information for genetic counseling, especially for families with a history of the disorder.
DPAGT1 Gene Glycosylation Disorder Type 1J Genetic Test Cost
The DPAGT1 gene glycosylation disorder Type 1J genetic test is a specialized diagnostic procedure designed to identify mutations in the DPAGT1 gene, which are associated with Congenital Disorders of Glycosylation (CDG). Type 1J CDG is a rare genetic condition that affects the normal process of adding sugar chains to proteins, a critical process for proper protein function. Symptoms of the disorder can vary widely among individuals but may include developmental delay, neurological issues, and problems with the digestive system, among others. This genetic test involves analyzing the patient's DNA to look for specific mutations in the DPAGT1 gene that are known to cause the disorder. Early diagnosis through genetic testing is crucial for managing symptoms and improving the quality of life for affected individuals. The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the DPAGT1 gene glycosylation disorder Type 1J genetic test at DNA Labs UAE is 4400 AED. This price may cover the collection of the sample, the genetic analysis, and the provision of a detailed report explaining the results. Patients interested in undergoing this test are advised to consult with a healthcare provider or a genetic counselor to understand the implications of the test results and explore potential treatment options.
