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RFX6 Gene Mitchell-Riley Syndrome Genetic Test Cost
The RFX6 Gene Mitchell-Riley Syndrome Genetic Test is a specialized diagnostic procedure designed to identify mutations in the RFX6 gene, which are associated with Mitchell-Riley Syndrome. This rare genetic disorder is characterized by a combination of congenital hypothyroidism, neonatal diabetes, pancreatic agenesis, and other developmental anomalies. Early and accurate diagnosis through this genetic test is crucial for the management and treatment of the condition, allowing for personalized care plans and interventions to improve patient outcomes. The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics and research. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expert interpretation that accompanies this advanced genetic testing service. By identifying the specific genetic alterations in the RFX6 gene, healthcare providers can better understand the syndrome's progression in each patient and tailor treatments to address their unique needs, significantly enhancing the quality of life for those affected by Mitchell-Riley Syndrome.
UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 Genetic Test Cost
The UQCC2 Gene Mitochondrial Complex III Deficiency Nuclear Type 7 Genetic Test is a specialized diagnostic examination conducted at DNA Labs UAE, designed to detect mutations in the UQCC2 gene. These mutations are associated with Mitochondrial Complex III Deficiency, Nuclear Type 7, a rare genetic disorder that affects the body's ability to generate energy. The test is crucial for identifying individuals who may be affected by this condition, which can lead to various symptoms ranging from muscle weakness, heart problems, to growth delays, depending on the severity of the deficiency. Given the complexity and the specific expertise required to perform and interpret this test, it is priced at 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by professionals skilled in genetic diagnostics, ensuring high accuracy and reliability of the test results. This genetic test is an essential tool for healthcare providers in diagnosing the condition early and accurately, allowing for appropriate management strategies to be implemented, enhancing the quality of life for affected individuals.
BCKDHA Gene Maple Syrup Urine Disease Type 1a Genetic Test Cost
The BCKDHA Gene Maple Syrup Urine Disease Type 1a Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the BCKDHA gene. These mutations are responsible for the most common form of Maple Syrup Urine Disease (MSUD), Type 1a. MSUD is a rare inherited metabolic disorder characterized by the body's inability to process certain amino acids properly, leading to a buildup of toxic substances that can cause severe neurological damage if not treated early. The test is particularly crucial for early diagnosis and management of the condition, which can significantly improve the quality of life and prognosis for affected individuals. Conducted through a simple blood sample, the genetic test searches for specific mutations in the BCKDHA gene that indicate the presence of MSUD Type 1a. Priced at 4400 AED, the test is an investment in health, especially for families with a history of the disorder or those who have had children with unexplained symptoms related to the disease. DNA Labs UAE provides this testing service with high accuracy and confidentiality, ensuring that individuals and families receive the necessary information for informed healthcare decisions.
DBT Gene Maple Syrup Urine Disease Type 2 Genetic Test Cost
The DBT Gene Maple Syrup Urine Disease Type 2 Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to detect mutations in the DBT gene associated with Maple Syrup Urine Disease (MSUD) Type 2. MSUD is a rare metabolic disorder characterized by the body's inability to process certain amino acids, leading to a distinctive sweet odor in the urine, akin to maple syrup, alongside potentially severe neurological damage if left untreated. The test aims to identify individuals carrying the genetic mutations responsible for this condition, facilitating early intervention and management strategies. Offered at a cost of 4400 AED, this genetic test represents a crucial tool for families with a history of the disease, or newborns showing symptoms, ensuring timely and appropriate care.
DLD Gene Maple Syrup Urine Disease Type 3 Genetic Test Cost
The DLD Gene Maple Syrup Urine Disease Type 3 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the DLD gene associated with Maple Syrup Urine Disease (MSUD) Type 3. MSUD is a rare inherited disorder characterized by the body's inability to process certain amino acids properly, leading to a buildup of toxic substances in the body. This condition is named for the distinctive sweet odor of affected infants' urine, resembling maple syrup. The Type 3 variant of MSUD, linked to mutations in the DLD gene, tends to have a more variable onset and can range from mild to severe in its presentation. The genetic test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the DLD gene that are known to cause MSUD Type 3. Identifying these mutations can confirm a diagnosis of MSUD Type 3, enabling timely intervention and management of the condition. At DNA Labs UAE, the cost for the DLD Gene Maple Syrup Urine Disease Type 3 Genetic Test is set at 4400 AED. This investment allows for a precise diagnosis, which is crucial for implementing appropriate dietary and medical management strategies to mitigate the effects of the disorder and improve the quality of life for affected individuals.
PPM1K Gene Maple Syrup Urine Disease Mild Variant Genetic Test Cost
The PPM1K Gene Maple Syrup Urine Disease Mild Variant Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the PPM1K gene associated with a milder form of Maple Syrup Urine Disease (MSUD). This genetic condition affects the body's ability to process certain amino acids, leading to a buildup that can cause harmful effects on the brain and other organs if not treated promptly. The test is crucial for early detection and management of the disease, particularly in individuals with a family history of MSUD or those showing symptoms of the disorder. By utilizing advanced genetic sequencing techniques, the test provides accurate results that can guide treatment and dietary recommendations to manage the condition effectively. The cost of the PPM1K Gene MSUD Mild Variant Genetic Test is 4400 AED, reflecting the comprehensive analysis and the specialized technology required to identify the specific gene mutations.
HNF4A Gene Maturity-onset Diabetes of the Young Type 1 Genetic Test Cost
The HNF4A gene maturity-onset diabetes of the young type 1 (MODY 1) genetic test is a specialized diagnostic procedure designed to identify mutations in the HNF4A gene, which are linked to a form of diabetes that typically manifests in adolescence or early adulthood. This form of diabetes, known as MODY 1, is characterized by a dysfunction in insulin production, leading to elevated blood sugar levels. Unlike the more common types of diabetes, MODY 1 has a strong genetic component and follows an autosomal dominant pattern of inheritance, meaning a single copy of the altered gene in each cell is sufficient to cause the disorder. The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED. By conducting this test, healthcare providers can make a precise diagnosis of MODY 1, enabling them to tailor treatment strategies to the individual's genetic profile. This personalized approach to diabetes management can significantly improve patient outcomes, helping to maintain blood sugar levels within a normal range and reduce the risk of diabetes-related complications. The test is recommended for individuals with a family history of MODY or those who exhibit symptoms of diabetes at an unusually young age and do not fit the typical profile of Type 1 or Type 2 diabetes.
INS Gene Maturity-onset Diabetes of the Young Type 10 Genetic Test Cost
The INS Gene Maturity-onset Diabetes of the Young Type 10 (MODY 10) genetic test is a sophisticated diagnostic tool designed to identify mutations in the INS gene, which are linked to MODY 10. This form of diabetes typically manifests at a young age and is characterized by a dysfunction in insulin production. Unlike other forms of diabetes, MODY 10 is inherited in an autosomal dominant pattern, meaning a mutation in just one copy of the gene can cause the condition. Conducted at DNA Labs UAE, this test is pivotal for individuals with a family history of MODY 10 or those exhibiting symptoms of diabetes at an early age without the typical risk factors associated with Type 1 or Type 2 diabetes. The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific genetic mutations in the INS gene. The cost of the INS Gene Maturity-onset Diabetes of the Young Type 10 genetic test at DNA Labs UAE is 4400 AED. This investment not only aids in the accurate diagnosis of MODY 10 but also facilitates personalized treatment plans that can significantly improve management of the condition. Early detection through genetic testing can empower individuals and their healthcare providers to take proactive steps in managing the disease, potentially improving quality of life and reducing the risk of diabetes-related complications.
