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GLYCTK Gene D-glyceric aciduria Genetic Test Cost
The GLYCTK Gene D-glyceric aciduria Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the GLYCTK gene, which are associated with D-glyceric aciduria, a rare metabolic disorder. This condition is characterized by elevated levels of D-glyceric acid in the urine, blood, and cerebrospinal fluid, potentially leading to various neurological symptoms, developmental delays, and metabolic complications. The test involves analyzing the patient's DNA to identify any genetic abnormalities in the GLYCTK gene that may indicate the presence of D-glyceric aciduria. Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers a crucial resource for individuals suspected of having this condition or for families with a history of metabolic disorders seeking a definitive diagnosis. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed report provided, which includes specific mutations identified and interpretation of the results in the context of the patient's health and family history. This information is vital for developing an effective management plan, offering genetic counseling, and understanding the risk of passing the condition to future generations.
AVPR2 Gene Diabetes insipidus nephrogenic X-linked Genetic Test Cost
The AVPR2 gene plays a crucial role in the body's water balance, and mutations in this gene can lead to X-linked nephrogenic diabetes insipidus (NDI). NDI is a rare condition characterized by the kidney's inability to properly respond to antidiuretic hormone (ADH), leading to excessive urination and thirst. This condition predominantly affects males, given its X-linked inheritance pattern. To diagnose this specific form of diabetes insipidus, genetic testing for mutations in the AVPR2 gene is conducted. DNA Labs UAE offers a comprehensive genetic test aimed at identifying mutations within the AVPR2 gene. This test is crucial for confirming the diagnosis of X-linked nephrogenic diabetes insipidus, guiding treatment plans, and providing valuable information for family planning. The test cost is set at 4400 AED. It involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the AVPR2 gene. The results of this test can help in the accurate diagnosis and management of the condition, allowing for tailored treatment strategies and improved quality of life for affected individuals. In summary, the AVPR2 gene diabetes insipidus nephrogenic X-linked genetic test offered by DNA Labs UAE is a specialized diagnostic tool essential for identifying mutations responsible for X-linked NDI, with a test cost of 4400 AED.
INSR Gene Diabetes mellitus insulin-resistant with acanthosis nigricans Genetic Test Cost
The "INSR Gene Diabetes Mellitus Insulin-Resistant with Acanthosis Nigricans Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the INSR gene. These mutations are closely associated with a rare form of diabetes mellitus characterized by insulin resistance and acanthosis nigricans, a skin condition marked by dark, velvety patches in body folds and creases. The test is crucial for individuals who exhibit symptoms of this condition or have a family history, as it helps in confirming the diagnosis, guiding treatment strategies, and informing family planning decisions. The cost of the test is 4400 AED, reflecting the advanced genetic analysis involved. By pinpointing specific genetic alterations, this test provides valuable insights into the patient's condition, enabling personalized medical care and management strategies to mitigate symptoms and improve quality of life.
GLIS3 Gene Diabetes mellitus neonatal Genetic Test Cost
The GLIS3 Gene Diabetes Mellitus Neonatal Genetic Test is a specialized diagnostic procedure designed to identify mutations in the GLIS3 gene, which are linked to the development of neonatal diabetes mellitus. This condition is a rare form of diabetes that appears in the first six months of a baby's life, characterized by high blood sugar levels due to the body's inability to produce enough insulin. The GLIS3 gene plays a critical role in pancreatic development and insulin gene expression. Mutations in this gene can lead to various health issues, including neonatal diabetes and thyroid problems. The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. The procedure involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the lab to detect any abnormalities in the GLIS3 gene. This test is crucial for early diagnosis and management of the condition, allowing for tailored treatment plans that can significantly improve the quality of life for affected infants. The cost of the GLIS3 Gene Diabetes Mellitus Neonatal Genetic Test at DNA Labs UAE is 4400 AED. Given the complexity of the analysis and the specialized technology required, this price reflects the comprehensive nature of the test, ensuring accurate and reliable results. Early detection through this genetic testing is invaluable for affected families, providing essential information for managing the condition effectively.
ABCC8 Gene Diabetes mellitus noninsulin-dependent Genetic Test Cost
The ABCC8 gene plays a crucial role in the regulation of insulin secretion in the pancreas. Mutations in this gene can lead to various forms of diabetes, including non-insulin-dependent diabetes mellitus (NIDDM), also known as Type 2 diabetes. The genetic test for the ABCC8 gene is a valuable diagnostic tool that helps in identifying individuals with a genetic predisposition to this form of diabetes. It is particularly useful for patients with a family history of Type 2 diabetes or those who exhibit potential symptoms of the condition but do not yet meet the criteria for a diabetes diagnosis based on glucose levels alone. Conducted at DNA Labs UAE, the test involves analyzing the patient's DNA to look for specific mutations in the ABCC8 gene that are known to affect insulin secretion. This information can be crucial for early intervention and personalized management plans, including lifestyle modifications and targeted therapies that may help in delaying or preventing the onset of Type 2 diabetes. The cost of the ABCC8 gene diabetes mellitus non-insulin-dependent genetic test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the specialized techniques used for genetic analysis and the expertise required to interpret the results accurately. Patients considering this test are encouraged to discuss it with their healthcare provider to understand its benefits and implications fully.
IGF2 Gene Diabetes IGF2 related Genetic Test Cost
The IGF2 gene, also known as Insulin-like Growth Factor 2, plays a crucial role in human growth and development. Research has indicated a connection between variations in the IGF2 gene and the risk of developing diabetes, particularly type 2 diabetes. This connection is rooted in the gene's influence on insulin production and its effect on body tissues' response to this hormone. To explore this genetic predisposition, DNA Labs UAE offers a specialized genetic test targeting the IGF2 gene to assess an individual's risk of developing diabetes related to IGF2 gene variations. This test is particularly valuable for those with a family history of diabetes or individuals who are seeking a comprehensive understanding of their genetic health profile regarding diabetes. The test involves a simple and non-invasive procedure, typically requiring a saliva or blood sample from the individual. Once the sample is collected, it undergoes a detailed analysis in the state-of-the-art facilities at DNA Labs UAE, where advanced genetic sequencing technologies are employed to identify any variations in the IGF2 gene that may increase the risk of diabetes. The cost of the IGF2 gene diabetes-related genetic test at DNA Labs UAE is 3200 AED. This price includes the full process of sample collection, genetic analysis, and a comprehensive report detailing the findings. The report not only provides information on the presence of any IGF2 gene variations but also offers insights into the individual's genetic predisposition to diabetes, empowering them with valuable information for proactive health management. Upon receiving their results, individuals are encouraged to consult with a healthcare provider or a genetic counselor to interpret the findings accurately and discuss potential lifestyle adjustments or interventions that may mitigate the risk of developing diabetes. This personalized approach to health monitoring underscores the importance of genetic testing in preventive healthcare strategies.
SLC26A3 Gene Diarrhea type 1 secretory chloride congenital Genetic Test Cost
The SLC26A3 gene plays a crucial role in the proper absorption and secretion of chloride ions in the intestines. Mutations in this gene can lead to Diarrhea type 1 secretory chloride congenital (DSC1), a disorder characterized by life-threatening diarrhea in infancy, which results from an inability to properly absorb chloride, leading to an imbalance of electrolytes and water in the body. Genetic testing for mutations in the SLC26A3 gene is crucial for diagnosing this condition, guiding treatment plans, and providing information for family planning. DNA Labs UAE offers a comprehensive genetic test for the SLC26A3 gene to identify mutations associated with DSC1. The test, which costs 4400 AED, involves collecting a DNA sample, usually through a blood draw or a cheek swab, and analyzing it to detect any genetic alterations in the SLC26A3 gene. This test is pivotal for early diagnosis and management of the condition, potentially saving lives and improving the quality of life for affected individuals and their families.
TRMT5 Gene Combined oxidative phosphorylation deficiency type 26 Genetic Test Cost
The TRMT5 Gene Combined Oxidative Phosphorylation Deficiency Type 26 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE. This test specifically targets the TRMT5 gene, which has been linked to Combined Oxidative Phosphorylation Deficiency Type 26 (COXPD26) - a rare genetic disorder that affects mitochondrial function, leading to a wide array of clinical manifestations including neurodevelopmental delays, muscle weakness, and metabolic complications. The test is designed to identify mutations in the TRMT5 gene, providing crucial information for the diagnosis, management, and treatment planning for affected individuals. By analyzing the patient's DNA, the test can confirm or rule out the presence of genetic alterations responsible for COXPD26, offering families and healthcare providers valuable insights into the condition. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, this test is priced at 4400 AED. The cost reflects the comprehensive nature of the analysis, which involves sophisticated sequencing technologies and expert interpretation of the results. For families facing the challenges of rare genetic disorders, this test represents a critical step towards understanding their condition and exploring potential therapeutic strategies.
