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BRIP1 Gene Fanconi anemia type J Genetic Test Cost
The BRIP1 Gene Fanconi Anemia Type J Genetic Test is a specialized diagnostic assessment conducted at DNA Labs UAE. This test is designed to detect mutations in the BRIP1 gene, which are linked to Fanconi anemia type J, a rare genetic disorder. Fanconi anemia is characterized by bone marrow failure, increased risk of cancer, and physical abnormalities. The identification of mutations in the BRIP1 gene through this test can aid in the diagnosis of the condition, allowing for early intervention and management strategies to be implemented. The test involves collecting a DNA sample, typically through a blood draw, which is then analyzed in the laboratory for the presence of genetic abnormalities associated with the condition. It is a crucial tool for families with a history of Fanconi anemia, individuals showing symptoms of the disease, or couples planning to have children who wish to understand their genetic risks. At DNA Labs UAE, the BRIP1 Gene Fanconi Anemia Type J Genetic Test is available for a cost of 4400 AED. The price reflects the comprehensive nature of the test, including the sophisticated techniques used for genetic analysis and the expertise required to interpret the results accurately. This test represents an important step towards personalized medicine, offering individuals and families critical information about their genetic health and guiding healthcare professionals in providing targeted care and support.
FANCL Gene Fanconi anemia type L Genetic Test Cost
The FANCL gene Fanconi anemia type L genetic test is a specialized diagnostic tool designed to identify mutations in the FANCL gene, which is associated with Fanconi anemia type L. Fanconi anemia is a rare genetic disorder that leads to bone marrow failure and increased risk of cancer. The test is crucial for early detection and management of the condition, allowing for appropriate medical interventions and genetic counseling for affected individuals and their families. Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw, and analyzing it for specific genetic mutations in the FANCL gene. The results can provide valuable information regarding the genetic makeup of the individual and the risk of developing Fanconi anemia type L. The cost of the FANCL gene Fanconi anemia type L genetic test is 4400 AED. This investment covers the sophisticated laboratory processes and expert analysis required to accurately identify mutations in the FANCL gene. For patients and families facing the possibility of Fanconi anemia, this test represents a critical step towards understanding their genetic health and making informed decisions about their care.
FANCM Gene Fanconi anemia type M Genetic Test Cost
The FANCM gene is associated with Fanconi anemia type M, a rare genetic disorder that affects the bone marrow and results in decreased production of all types of blood cells. This condition can lead to physical abnormalities, organ defects, and an increased risk of certain cancers. The FANCM gene plays a crucial role in the body's ability to repair damaged DNA, and mutations in this gene can disrupt this critical process, leading to the symptoms and complications associated with Fanconi anemia. To diagnose Fanconi anemia type M and identify mutations in the FANCM gene, a genetic test is available at DNA Labs UAE. This test involves analyzing the patient's DNA to look for mutations in the FANCM gene that are known to cause the condition. It is a vital tool for confirming the diagnosis, understanding the disease's progression, and making informed decisions about treatment options. The cost of the FANCM gene Fanconi anemia type M genetic test at DNA Labs UAE is 4400 AED. This test is crucial for individuals with a family history of Fanconi anemia or those presenting symptoms consistent with the disorder. By identifying the specific genetic mutation, healthcare providers can offer personalized care and management strategies to improve the quality of life for affected individuals.
PALB2 Gene Fanconi anemia type N Genetic Test Cost
The PALB2 Gene Fanconi Anemia Type N Genetic Test is a specialized diagnostic tool designed to identify mutations in the PALB2 gene, which are linked to the development of Fanconi anemia type N, a rare and inherited form of anemia that leads to decreased production of blood cells, increased risk of cancer, and other serious health problems. This test is crucial for individuals with a family history of the condition or those exhibiting symptoms, as early detection can significantly influence management and treatment strategies. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, typically through a blood draw, and analyzing it for specific mutations in the PALB2 gene. The accuracy and reliability of the test results from DNA Labs UAE make it a valuable resource for affected families and their healthcare providers. The cost of the PALB2 Gene Fanconi Anemia Type N Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the test provides essential information for the genetic counseling process, guiding both preventative measures and therapeutic interventions for individuals at risk. This test represents a critical step towards personalized medicine, offering hope and options for those facing the challenges of Fanconi anemia type N.
SLX4 Gene Fanconi anemia type P Genetic Test Cost
The SLX4 gene plays a critical role in DNA repair mechanisms and is closely associated with Fanconi anemia type P, a rare genetic disorder. This condition can lead to various physical abnormalities, bone marrow failure, and increased cancer risk. Identifying mutations in the SLX4 gene is crucial for diagnosing Fanconi anemia type P, enabling early intervention and management of the condition. DNA Labs UAE offers a specialized genetic test targeting the SLX4 gene to identify mutations linked to Fanconi anemia type P. The test is conducted with high precision, ensuring reliable results for patients and their families. With a cost of 4400 AED, the test is an investment in understanding and managing this genetic condition more effectively. By opting for this test, individuals can gain insights into their genetic makeup, leading to informed decisions regarding their health and the possibility of passing the condition to future generations.
XRCC2 Gene Fanconi anemia XRCCR2 related Genetic Test Cost
The XRCC2 Gene Fanconi Anemia XRCCR2 Related Genetic Test is a specialized diagnostic tool designed to identify mutations in the XRCC2 gene, which are implicated in a rare and complex condition known as Fanconi anemia. This condition is genetically inherited and affects the body's ability to repair DNA, leading to increased risks of certain cancers, bone marrow failure, and developmental abnormalities. The test is crucial for individuals with a family history of Fanconi anemia or related symptoms, as early detection can significantly impact management and treatment options. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers a comprehensive analysis of the XRCC2 gene to pinpoint any genetic alterations. Understanding these genetic variations can provide valuable insights into the condition's prognosis, potential complications, and guide personalized treatment plans. Additionally, it can inform family planning decisions for those carrying the mutation. The cost of the XRCC2 Gene Fanconi Anemia XRCCR2 Related Genetic Test is set at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify and interpret genetic mutations associated with this condition. Given the complexity of Fanconi anemia and its potential implications for affected individuals and their families, this test represents a critical step towards proactive health management and informed medical decision-making.
SLC2A2 Gene Fanconi-Bickel syndrome Genetic Test Cost
The SLC2A2 gene plays a crucial role in the body, encoding for the GLUT2 protein which is vital for glucose transport into cells. Mutations in the SLC2A2 gene can lead to Fanconi-Bickel syndrome, a rare genetic disorder characterized by impaired glucose and galactose metabolism, leading to various symptoms including growth retardation, rickets, and kidney issues among others. To diagnose this condition, a genetic test focusing on the SLC2A2 gene can be performed. This test is available at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services. The test specifically looks for mutations in the SLC2A2 gene that are indicative of Fanconi-Bickel syndrome. The cost of the SLC2A2 gene Fanconi-Bickel syndrome genetic test at DNA Labs UAE is 4400 AED. This price includes the full testing procedure and a detailed report of the findings. The test is carried out by experienced professionals who ensure the accuracy and confidentiality of the results, providing crucial information for the diagnosis, treatment, and management of Fanconi-Bickel syndrome.
ASAH1 Gene Farber disease Genetic Test Cost
The ASAH1 gene plays a crucial role in the development of Farber disease, a rare genetic disorder that affects the body's ability to break down certain fats, leading to harmful accumulation in various tissues and organs. This condition is inherited in an autosomal recessive pattern and is characterized by symptoms such as joint swelling, voice hoarseness, and in severe cases, neurological impairment. To diagnose Farber disease and assess the risk of passing it on to future generations, a genetic test targeting the ASAH1 gene can be conducted. This test involves analyzing DNA to identify mutations in the ASAH1 gene that are known to cause the disease. It is a crucial step for families with a history of Farber disease or for individuals showing symptoms of the disorder. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic testing service. The cost of the ASAH1 Gene Farber Disease Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test provides valuable information for affected individuals and their families, aiding in the management of the disease and informing decisions regarding family planning. It's important for patients to consult with a healthcare provider or a genetic counselor before and after undergoing genetic testing to understand the implications of the results fully.
