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ABCA1 Gene HDL Deficiency Type 2 Genetic Test Cost
The ABCA1 Gene HDL Deficiency Type 2 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the ABCA1 gene. This gene plays a crucial role in the regulation of high-density lipoprotein (HDL) cholesterol levels in the bloodstream. Mutations in the ABCA1 gene can lead to Tangier disease or familial HDL deficiency, conditions characterized by extremely low levels of HDL cholesterol, which is often referred to as "good" cholesterol due to its role in removing other forms of cholesterol from the bloodstream. The test is critical for individuals with a family history of HDL deficiency or premature cardiovascular disease, as it can provide vital information for managing health risks associated with these conditions. Conducted through a blood sample, the genetic analysis focuses on identifying specific mutations in the ABCA1 gene that are known to contribute to HDL deficiency type 2. The cost of the ABCA1 Gene HDL Deficiency Type 2 Genetic Test at DNA Labs UAE is 4400 AED. This investment in health allows individuals to take proactive steps in managing their cardiovascular health through personalized medical guidance and lifestyle adjustments based on their genetic predisposition. Early detection through this genetic test can be instrumental in implementing preventive measures to mitigate the risk of heart disease and other related conditions.
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.
PHKG2 Gene Glycogen Storage Disease Type 9C Genetic Test Cost
The PHKG2 gene plays a crucial role in the body's glycogen metabolism, a process essential for storing and mobilizing energy. Mutations in the PHKG2 gene can lead to Glycogen Storage Disease Type 9C (GSD9C), a rare genetic disorder characterized by an inability to properly break down glycogen, leading to its accumulation in various tissues, particularly the liver. This can result in symptoms such as hepatomegaly (enlarged liver), hypoglycemia (low blood sugar), and growth retardation among affected individuals. To diagnose GSD9C, genetic testing is essential. DNA Labs UAE offers a specialized genetic test targeting the PHKG2 gene to confirm the diagnosis of Glycogen Storage Disease Type 9C. This test involves analyzing the patient's DNA to identify mutations in the PHKG2 gene that are indicative of GSD9C. It is a crucial step for affected families, as it can help in managing the condition through dietary interventions and monitoring, improving the quality of life for those affected. The cost of the PHKG2 Gene Glycogen Storage Disease Type 9C Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to accurately diagnose this condition, enabling targeted management strategies and potentially reducing the risk of complications associated with GSD9C.
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.
DPM1 Gene Glycosylation Disorder Type 1E Genetic Test Cost
The "DPM1 Gene Glycosylation Disorder Type 1E Genetic Test" is a specialized diagnostic assessment offered by DNA Labs UAE, designed to detect mutations in the DPM1 gene, which are responsible for a rare genetic condition known as Congenital Disorders of Glycosylation Type 1E (CDG-1E). This condition affects the normal process of glycosylation, a critical biological process where sugars are attached to proteins and lipids, impacting various bodily functions. CDG-1E can lead to a wide range of symptoms, including developmental delay, neurological issues, and abnormalities in liver function. Early and accurate diagnosis through genetic testing is crucial for managing the condition, as it can guide treatment options and help in understanding the prognosis. The test is priced at 4400 AED and is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services. The test involves analyzing the patient's DNA sample for specific mutations in the DPM1 gene, providing a definitive diagnosis for affected individuals. This test is particularly important for families with a history of the condition or those exhibiting symptoms related to glycosylation disorders.
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.