The G6PC gene plays a crucial role in the body's glucose metabolism. Mutations in this gene are responsible for a condition known as Von Gierke disease, also known as Glycogen Storage Disease Type Ia (GSD Ia). This inherited disorder affects the liver and kidneys' ability to regulate blood sugar levels, leading to symptoms such as hypoglycemia, lactic acidosis, hyperuricemia, and growth retardation.
To diagnose Von Gierke disease and confirm a genetic mutation in the G6PC gene, a genetic test is available. DNA Labs UAE offers this specific test, providing a crucial tool for individuals suspecting they or their family members may have this condition. The test involves analyzing the DNA to identify mutations in the G6PC gene that are indicative of Von Gierke disease.
The cost of the G6PC Gene Von-Gierke Disease Genetic Test at DNA Labs UAE is 4400 AED. This test is essential for accurate diagnosis, enabling targeted management and treatment plans for affected individuals. It also provides valuable information for family planning and the assessment of risk in future offspring.
The ATP7B gene Wilson disease genetic test is a diagnostic tool used to identify mutations in the ATP7B gene, which are responsible for Wilson disease, a rare autosomal recessive disorder. This genetic condition leads to excessive accumulation of copper in the body, affecting the liver, brain, and other organs. Early detection through genetic testing is crucial for managing symptoms and preventing severe complications. The test involves analyzing the DNA to look for specific mutations in the ATP7B gene that are known to cause Wilson disease.
Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services, the ATP7B gene test is available for a cost of 4400 AED. This comprehensive test offers individuals and families critical information regarding the genetic predisposition to Wilson disease, enabling timely intervention and appropriate management strategies. By choosing DNA Labs UAE for this test, patients can expect accurate results, professional confidentiality, and guidance on the implications of the test outcomes.
The LIPA Gene Wolman Disease Genetic Test is a specialized diagnostic tool designed to identify mutations in the LIPA gene, which are responsible for Wolman disease. This rare genetic disorder is characterized by the body's inability to properly break down fats, leading to significant health issues such as malabsorption, liver dysfunction, and adrenal gland problems. Early detection through this genetic test can be crucial for managing symptoms and improving the quality of life for affected individuals.
The test is performed by DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the LIPA Gene Wolman Disease Genetic Test is set at 4400 AED. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any mutations in the LIPA gene. The results from this test can provide valuable information for families and healthcare providers, enabling them to make informed decisions regarding treatment and care for those diagnosed with Wolman disease.
The XDH Gene Xanthinuria Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in the XDH gene that are associated with Xanthinuria Type 1. This rare genetic disorder impacts the body's ability to metabolize purines, leading to an accumulation of xanthine, which can result in kidney stones, kidney failure, and occasionally muscle disease. The test involves analyzing the patient's DNA to identify any genetic alterations in the XDH gene that might lead to the condition. With a cost of 4400 AED, the test provides crucial information for the accurate diagnosis and management of Xanthinuria Type 1, enabling targeted treatment plans and lifestyle adjustments to mitigate the risk of complications associated with this disorder. DNA Labs UAE, known for its advanced genetic testing services, offers this test as part of its commitment to providing comprehensive diagnostic solutions for rare genetic conditions.
The MOCOS gene xanthinuria type 2 genetic test is a specialized diagnostic procedure aimed at detecting mutations in the MOCOS gene, which are responsible for xanthinuria type 2, a rare metabolic disorder. This condition is characterized by an inability to properly metabolize purines, leading to an accumulation of xanthine in the body. Such accumulation can result in various health issues, including kidney stones and potentially leading to kidney failure if left untreated.
The test is performed by DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is set at 4400 AED, reflecting the sophisticated nature of the diagnostic process and the specialized expertise required to accurately interpret the results. This test is crucial for individuals suspected of having xanthinuria type 2 or for those with a family history of the condition, as early detection can significantly improve management and treatment outcomes.
The COL4A4 gene plays a critical role in the formation of collagen IV, a major component of the basement membranes in various tissues, including the kidney, inner ear, and eye. Mutations in the COL4A4 gene can lead to Alport syndrome, a genetic disorder characterized by kidney disease, hearing loss, and eye abnormalities. Alport syndrome can be inherited in an autosomal recessive manner, meaning that an individual must inherit two copies of the mutated gene, one from each parent, to be affected.
Genetic testing for mutations in the COL4A4 gene is crucial for the diagnosis and management of Alport syndrome. This test can confirm the diagnosis, guide treatment decisions, and help in assessing the risk of passing the condition on to future generations. DNA Labs UAE offers a comprehensive genetic test for the COL4A4 gene to identify mutations associated with Alport syndrome in an autosomal recessive inheritance pattern. The cost of the test is 4400 AED.
By conducting this test, healthcare providers and patients can gain valuable insights into the genetic basis of the condition, enabling personalized treatment plans and informed family planning decisions. DNA Labs UAE utilizes advanced genetic sequencing technologies to ensure accurate and reliable results, providing crucial information for the management of individuals with Alport syndrome and their families.
The COL4A5 gene Alport syndrome X-linked genetic test is a specialized diagnostic procedure aimed at identifying mutations in the COL4A5 gene, which is pivotal in diagnosing Alport syndrome. This condition is an inherited disorder that primarily affects the kidneys, leading to progressive loss of kidney function, and can also impact the ears and eyes. Since Alport syndrome is X-linked, it predominantly affects males, who are likely to experience more severe symptoms compared to females.
The test involves analyzing the patient's DNA to look for abnormalities in the COL4A5 gene, which is responsible for the production of a type of collagen essential for the normal functioning of the kidneys, ears, and eyes. Identifying mutations in this gene can confirm a diagnosis of Alport syndrome, enabling early intervention and management of the condition.
Conducted at DNA Labs UAE, the test cost is set at 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology and staffed by professionals skilled in genetic testing, ensuring accurate and reliable results. Opting for this test at DNA Labs UAE provides patients and their families with critical information for managing Alport syndrome, including insights into the disease's progression, potential treatments, and the risk of passing the condition to future generations.
The DIAPH3 gene is associated with a form of auditory neuropathy, a condition characterized by a disruption in the transmission of sound from the inner ear to the brain, leading to hearing loss. This condition can be inherited in an autosomal dominant pattern, meaning a mutation in just one of the two copies of the gene is sufficient to cause the disorder. Genetic testing for mutations in the DIAPH3 gene can provide a definitive diagnosis of this form of auditory neuropathy, guiding treatment and management decisions for affected individuals and their families.
DNA Labs UAE offers a genetic test specifically targeting the DIAPH3 gene to identify mutations responsible for autosomal dominant auditory neuropathy. The test involves analyzing the patient's DNA, usually obtained through a blood sample, to search for abnormalities within the DIAPH3 gene that are known to cause the condition. This test is particularly useful for individuals showing symptoms of auditory neuropathy or those with a family history of the condition, as it can confirm the diagnosis and assist in understanding the risk of passing the condition to future generations.
The cost of the DIAPH3 gene auditory neuropathy autosomal dominant genetic test at DNA Labs UAE is 4400 AED. This price includes the collection of the sample, the genetic analysis, and a comprehensive report of the findings. It's important for patients considering this test to consult with a healthcare provider or a genetic counselor to discuss the implications of the test results for themselves and their family members.
The EYA1 Gene Branchiootorenal Syndrome Type 1 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the EYA1 gene, which are associated with Branchiootorenal (BOR) syndrome type 1. This syndrome is a rare genetic disorder characterized by the combination of branchial arch anomalies, hearing loss, and renal malformations. The test plays a crucial role in confirming the diagnosis, allowing for early intervention and management of the condition. Priced at 4400 AED, this test is a critical tool for families with a history of BOR syndrome, aiming to provide them with crucial information regarding their genetic status and the potential risks of passing the condition to their offspring. By leveraging advanced genetic testing techniques, DNA Labs UAE ensures accurate and reliable results, contributing to the effective care and counseling of affected individuals and their families.
The IARS2 gene plays a critical role in human development and health, with mutations in this gene being associated with a rare but complex syndrome. This condition is characterized by a constellation of symptoms including cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia. These symptoms can significantly affect the quality of life, making early diagnosis and management crucial.
To aid in the diagnosis of this condition, DNA Labs UAE offers a genetic test specifically designed to analyze the IARS2 gene for mutations. This test is a valuable tool for clinicians and families seeking answers to unexplained symptoms related to the mentioned conditions. The genetic test can help in confirming the diagnosis, which is essential for the proper management and treatment of the affected individuals.
The cost of the IARS2 gene test at DNA Labs UAE is 4400 AED. This investment can provide critical information for the affected individuals and their families, guiding them towards appropriate interventions and potentially improving outcomes. It's important for patients considering this test to consult with a healthcare professional or a genetic counselor to understand the implications of the test results and to ensure it's the right step for their specific situation.
