The PTPN23 gene plays a significant role in ciliogenesis, the process by which cilia are formed. Cilia are small, hair-like structures on the surface of cells that are crucial for various bodily functions, including movement, sensory processes, and signaling pathways. Abnormalities in ciliogenesis can lead to a range of disorders known as ciliopathies, which can affect multiple systems in the body, such as the respiratory system, the nervous system, and the reproductive system.
To diagnose disorders related to ciliogenesis, particularly those associated with mutations in the PTPN23 gene, genetic testing is utilized. DNA Labs UAE offers a specific genetic test that identifies mutations in the PTPN23 gene, which can help in diagnosing the underlying cause of ciliogenesis-related disorders. This test is particularly important for individuals presenting symptoms of ciliopathies or those with a family history of such conditions.
The cost of the PTPN23 gene ciliogenesis-related disorder genetic test at DNA Labs UAE is 4400 AED. This test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any genetic mutations in the PTPN23 gene. The results of this test can provide valuable information for diagnosis, prognosis, and management of ciliogenesis-related disorders, enabling targeted treatment and genetic counseling for affected individuals and their families.
The CATSPER2 gene plays a crucial role in human biology, particularly in the functioning of sperm cells and the inner ear's sensory cells. Mutations in the CATSPER2 gene can lead to a unique combination of symptoms, primarily characterized by deafness and male infertility. This condition underscores the gene's significance in both auditory processes and male reproductive capabilities.
DNA Labs UAE offers a specialized genetic test aimed at identifying mutations in the CATSPER2 gene. This test is essential for individuals who may be experiencing symptoms related to the gene's dysfunction, such as hearing impairments and challenges with male fertility. By undergoing this genetic analysis, individuals can gain valuable insights into their condition, enabling them to explore targeted treatment options and family planning strategies.
The test is priced at 4400 AED, reflecting the comprehensive nature of the analysis, which includes detailed genetic sequencing and interpretation by medical genetics experts. Conducted in a state-of-the-art laboratory setting, the test ensures accuracy and reliability, providing crucial information for affected individuals and their families. Through this testing, DNA Labs UAE contributes to the broader understanding of CATSPER2-related conditions, offering hope and direction for those impacted by its mutations.
The GJB2 gene is crucial for the proper function of cells in the inner ear and skin. Mutations in this gene can lead to a rare condition characterized by deafness, abnormal thickening of the skin (keratopachydermia), and constrictions of fingers and toes. The GJB2 Gene Deafness with Keratopachydermia and Constrictions of Fingers and Toes Genetic Test is a specialized diagnostic tool available at DNA Labs UAE. This test is designed to identify mutations in the GJB2 gene that are responsible for this condition. With a cost of 4400 AED, the test provides crucial information for the diagnosis and management of affected individuals, guiding treatment plans and offering families genetic counseling options. DNA Labs UAE utilizes state-of-the-art genetic testing technologies to ensure accurate and reliable results for patients and their healthcare providers.
The SFTPB gene plays a crucial role in the production of pulmonary surfactant, a substance essential for lung function by reducing surface tension in the alveoli, thus preventing lung collapse. Mutations in the SFTPB gene can lead to surfactant metabolism dysfunction type 1, a rare genetic disorder characterized by respiratory distress and lung disease in infants and young children.
To diagnose this condition, a genetic test targeting the SFTPB gene can be conducted. This test is available at DNA Labs UAE, a facility known for its advanced genetic testing services. The test specifically looks for mutations in the SFTPB gene that are known to cause surfactant metabolism dysfunction type 1. Early diagnosis through this test can be crucial for the management and treatment of the disorder, potentially improving the quality of life and outcomes for affected individuals.
The cost of the SFTPB gene surfactant metabolism dysfunction type 1 genetic test at DNA Labs UAE is 4400 AED. This price includes the collection of a DNA sample, usually through a blood draw or cheek swab, the analysis of the gene for specific mutations, and a comprehensive report of the findings. The report not only provides diagnostic information but may also offer insights into potential treatment strategies based on the genetic findings. This test is an invaluable tool for families with a history of lung disease or for newborns showing symptoms of respiratory distress, offering them a path towards understanding and managing the condition effectively.
The "SFTPC Gene Surfactant Metabolism Dysfunction Type 2 Genetic Test" is a specialized diagnostic procedure available at DNA Labs UAE, aimed at detecting mutations in the SFTPC gene. This gene plays a critical role in the production of pulmonary surfactant, a substance essential for lung function, which reduces the surface tension within the alveoli to prevent lung collapse. Mutations in the SFTPC gene can lead to Surfactant Metabolism Dysfunction Type 2, a rare pulmonary disorder that can cause respiratory distress and interstitial lung disease, particularly in infants and young children.
The test is crucial for individuals with a clinical history suggestive of surfactant metabolism dysfunction, as it provides definitive genetic evidence of the disorder. Early diagnosis through this genetic testing allows for timely intervention and management strategies to address the pulmonary conditions associated with the disorder, potentially improving the quality of life for affected individuals.
Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, the test costs 4400 AED. This investment covers the comprehensive analysis required to detect the presence of mutations in the SFTPC gene, offering invaluable insights for affected families and their healthcare providers. By opting for this test at DNA Labs UAE, patients and their families can access cutting-edge genetic analysis with the potential to significantly impact treatment decisions and outcomes for those diagnosed with Surfactant Metabolism Dysfunction Type 2.
The ABCA3 Gene Surfactant Metabolism Dysfunction Type 3 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the ABCA3 gene, which are linked to Surfactant Metabolism Dysfunction Type 3. This condition is a rare genetic disorder that affects the lungs, leading to severe respiratory problems from birth or early infancy. The ABCA3 gene plays a crucial role in the production of surfactant, a substance essential for lung function, by helping to transport and process lipids within cells. Mutations in this gene can disrupt surfactant production and function, leading to lung disease.
The test is priced at 4400 AED and involves analyzing the patient's DNA to detect mutations in the ABCA3 gene. It is a critical tool for diagnosing this condition, enabling healthcare providers to tailor treatment plans according to the specific genetic mutation present. Early and accurate diagnosis through this genetic test can significantly impact the management and prognosis of individuals with Surfactant Metabolism Dysfunction Type 3, offering hope for better outcomes. DNA Labs UAE provides this test as part of its comprehensive genetic testing services, employing state-of-the-art technology to ensure accurate and reliable results.
The CSF2RB gene is integral to the proper functioning of surfactant metabolism in the human body. Surfactant is a substance that prevents the collapse of the lungs by reducing the surface tension of fluids that coat the lung surface. Mutations in the CSF2RB gene can lead to surfactant metabolism dysfunction type 5, a rare genetic condition that can affect an individual's respiratory function from infancy or early childhood.
To diagnose this condition, a specific genetic test targeting the CSF2RB gene can be conducted. This test is designed to identify mutations in the CSF2RB gene that are responsible for surfactant metabolism dysfunction type 5. Early diagnosis through genetic testing is crucial as it can guide appropriate treatment and management strategies to improve the quality of life for affected individuals.
In the United Arab Emirates, this genetic test is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the CSF2RB gene surfactant metabolism dysfunction type 5 genetic test at DNA Labs UAE is 4400 AED. This test is a valuable resource for families with a history of respiratory or genetic conditions, providing them with crucial information for managing their health and making informed decisions about their medical care.
The ABCA1 gene plays a critical role in the regulation of cellular cholesterol and phospholipid transport. Mutations in the ABCA1 gene are associated with Tangier disease, a rare genetic disorder characterized by severely reduced levels of high-density lipoprotein (HDL) in the blood, alongside the accumulation of cholesterol in various tissues. This condition can lead to a spectrum of clinical manifestations, including neuropathy, hepatosplenomegaly, and an increased risk of cardiovascular disease.
Genetic testing for Tangier disease involves analyzing the ABCA1 gene to identify mutations that cause the disorder. DNA Labs UAE offers a comprehensive genetic test for this purpose, aimed at individuals who have a clinical diagnosis or are at risk due to family history. The test can provide valuable information for diagnosis, prognosis, and guiding management and treatment decisions for affected individuals and their families.
The cost of the ABCA1 gene Tangier disease genetic test at DNA Labs UAE is 4400 AED. This investment in health can offer crucial insights into the genetic basis of the condition, enabling targeted interventions and personalized medical care. By identifying carriers within a family, the test also assists in genetic counseling, helping families understand the risk of passing the condition to future generations.
The HEXA Gene Tay-Sachs Disease Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the HEXA gene, which are responsible for Tay-Sachs disease, a rare, inherited disorder. Tay-Sachs disease affects the nerve cells in the brain and spinal cord, leading to severe neurological impairment. This genetic test is crucial for identifying carriers of the gene mutation and for prenatal screening, thereby helping in managing the disease's progression and planning for future pregnancies.
Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a comprehensive analysis of the HEXA gene to identify any abnormalities that may indicate the presence of Tay-Sachs disease. The test cost is set at 3200 AED, reflecting the sophisticated technology and expert analysis involved in providing accurate and reliable results. By opting for this test, individuals can gain valuable insights into their genetic makeup, enabling informed decisions about their health and that of their potential offspring.
The GM2A Gene Tay-Sachs Disease AB Variant Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the GM2A gene, which are linked to the AB variant of Tay-Sachs disease. This rare, inherited disorder affects the central nervous system and is characterized by a progressive deterioration of mental and physical abilities. The test plays a crucial role in early detection and management of the condition, providing essential information for genetic counseling and planning for affected families. The procedure involves analyzing the patient's DNA to look for specific genetic alterations associated with the disease, offering a high degree of accuracy in diagnosing this variant of Tay-Sachs disease. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify the genetic markers associated with this condition. By opting for this test at DNA Labs UAE, individuals can gain valuable insights into their genetic health, enabling informed medical and personal decisions.
