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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.
TSFM Gene Combined oxidative phosphorylation deficiency type 3 Genetic Test Cost
The TSFM gene is associated with a rare condition known as Combined Oxidative Phosphorylation Deficiency Type 3 (COXPD3). This genetic disorder affects the body's ability to produce energy efficiently, leading to a range of symptoms that can include muscle weakness, heart problems, and developmental delays, among others. The condition is inherited in an autosomal recessive pattern, meaning that a child must inherit two copies of the mutated gene, one from each parent, to be affected. To diagnose this condition, a specific genetic test targeting the TSFM gene can be performed. This test looks for mutations in the TSFM gene that are known to cause Combined Oxidative Phosphorylation Deficiency Type 3. It is a crucial step in confirming the diagnosis, understanding the disease's progression, and exploring potential treatment options. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic testing service. The cost of the TSFM gene test is 4400 AED. Conducting this test at DNA Labs UAE ensures that individuals and families receive accurate and comprehensive results, thanks to the lab's expertise in genetic diagnostics and its use of advanced testing technologies. This information is vital for affected families to make informed decisions about their health and to seek appropriate medical interventions.
TUFM Gene Combined oxidative phosphorylation deficiency type 4 Genetic Test Cost
The TUFM gene plays a crucial role in the mitochondrial translation process, essential for the production of proteins that are critical components of the mitochondrial respiratory chain. Mutations in the TUFM gene can lead to Combined Oxidative Phosphorylation Deficiency Type 4 (COXPD4), a rare genetic disorder that affects multiple systems in the body, leading to severe clinical manifestations including lactic acidosis, developmental delay, and possible heart and liver involvement. To diagnose this condition, genetic testing for the TUFM gene mutation is crucial. DNA Labs UAE offers a specialized test designed to identify mutations in the TUFM gene associated with COXPD4. This test is a vital tool for clinicians in the diagnosis and management of patients suspected of having this rare disorder. The cost of the test is 4400 AED, reflecting the comprehensive analysis and the specialized technology employed to detect these mutations accurately. By confirming the presence of a TUFM gene mutation, this test helps in guiding treatment decisions, provides information on the prognosis, and assists in genetic counseling for affected families. It is a critical step towards personalized medicine for patients with COXPD4, enabling targeted interventions and support to improve their quality of life.
MRPS22 Gene Combined oxidative phosphorylation deficiency type 5 Genetic Test Cost
The MRPS22 Gene Combined Oxidative Phosphorylation Deficiency Type 5 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the MRPS22 gene. These mutations are responsible for Combined Oxidative Phosphorylation Deficiency Type 5 (COXPD5), a rare genetic disorder that affects mitochondrial function, leading to a wide range of symptoms including developmental delay, muscle weakness, and metabolic abnormalities. Mitochondria are the powerhouses of the cell, and their dysfunction can have widespread effects on the body's energy production. This test is crucial for the accurate diagnosis of COXPD5, allowing for a better understanding of the condition and facilitating tailored treatment and management plans for affected individuals. The procedure involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific mutations in the MRPS22 gene. The cost of the MRPS22 Gene Combined Oxidative Phosphorylation Deficiency Type 5 Genetic Test at DNA Labs UAE is 4400 AED. This investment includes the comprehensive analysis and detailed reporting necessary to understand the genetic basis of the condition, providing essential information for patients, families, and healthcare providers in managing the disorder.
AIFM1 Gene Combined oxidative phosphorylation deficiency type 6 Genetic Test Cost
The AIFM1 gene plays a crucial role in the process of oxidative phosphorylation, a critical pathway for energy production within cells. Mutations in the AIFM1 gene can lead to Combined Oxidative Phosphorylation Deficiency Type 6 (COXPD6), a rare genetic disorder that affects multiple body systems and can result in a wide range of symptoms, including muscle weakness, neurological deficits, and developmental delays. To diagnose this condition, genetic testing is available at DNA Labs UAE. The test specifically looks for mutations in the AIFM1 gene that are associated with COXPD6. It is a crucial step for affected individuals and their families to understand the underlying genetic cause of the condition, which can inform treatment decisions and help in assessing the risk for future children. The cost of the AIFM1 gene test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the presence of mutations in the AIFM1 gene. Given the complexity of genetic testing and the significant information it provides, the test is a valuable tool for individuals and families dealing with the implications of COXPD6.
C12ORF65 Gene Combined oxidative phosphorylation deficiency type 7 Genetic Test Cost
The C12ORF65 gene plays a critical role in the proper functioning of the mitochondrial translation machinery, which is essential for the synthesis of proteins involved in oxidative phosphorylation. Mutations in this gene can lead to Combined Oxidative Phosphorylation Deficiency Type 7 (COXPD7), a rare genetic disorder characterized by a wide range of symptoms, including muscle weakness, neurological deficits, and developmental delays, among others. Early and accurate diagnosis of COXPD7 is crucial for managing the symptoms and improving the quality of life of affected individuals. DNA Labs UAE offers a genetic test specifically designed to identify mutations in the C12ORF65 gene, aiding in the diagnosis of COXPD7. The test is conducted using a sample of the patient's DNA, usually obtained through a blood draw or a cheek swab. The procedure involves analyzing the genetic material for specific mutations known to be associated with the condition. The cost of the C12ORF65 gene test at DNA Labs UAE is 4400 AED. This comprehensive test is a critical tool for healthcare providers in diagnosing Combined Oxidative Phosphorylation Deficiency Type 7, allowing for timely intervention and management strategies tailored to the individual's specific needs. By offering this test, DNA Labs UAE contributes to the enhanced understanding and treatment of rare genetic disorders, supporting patients and their families in navigating these challenging conditions.