CSF Leakage Evaluation Nasal Ear Discharge Test is a specialized diagnostic procedure aimed at identifying the presence of cerebrospinal fluid (CSF) in nasal or ear discharge. This test is particularly crucial for individuals who have symptoms suggestive of a CSF leak, such as clear fluid drainage from the nose or ear, especially if it increases with sneezing, coughing, or straining. CSF leaks can result from trauma, surgical procedures, or can be spontaneous, and it's important to diagnose them promptly to prevent complications like infections.
The test involves collecting a sample of the discharge and analyzing it for the presence of beta-2 transferrin, a protein that is uniquely found in cerebrospinal fluid, making it a definitive marker for CSF leakage. This non-invasive test provides a reliable means of confirming or ruling out a breach between the cranial cavity and the nasal or ear passages.
At DNA Labs UAE, the CSF Leakage Evaluation Nasal Ear Discharge Test is available for a cost of 1290 AED. DNA Labs UAE is equipped with state-of-the-art facilities and employs highly skilled professionals to conduct this test, ensuring accurate and reliable results. The test is performed under strict quality control measures, adhering to the highest standards of diagnostic testing. Patients opting for this test at DNA Labs UAE can expect professional service, confidentiality, and timely results, facilitating prompt and appropriate management of the condition.
The DRPLA (Dentatorubral-Pallidoluysian Atrophy) Gene Analysis Test is a specialized diagnostic procedure available at DNA Labs UAE, aimed at detecting mutations in the ATN1 gene, which are responsible for the development of Dentatorubral-Pallidoluysian Atrophy (DRPLA). DRPLA is a rare, hereditary neurodegenerative disorder that affects the brain, leading to a wide range of symptoms including involuntary movements, mental and emotional problems, and a decline in motor skills.
This genetic test involves analyzing the patient's DNA to identify the specific mutations in the ATN1 gene, offering crucial information for the diagnosis, management, and understanding of the patient's condition. The process is designed to be both accurate and comprehensive, ensuring a reliable diagnosis for affected individuals or those at risk of developing the condition.
At DNA Labs UAE, the DRPLA Gene Analysis Test is priced at 1290 AED. The cost reflects the sophisticated technology and expertise required to perform this detailed genetic analysis. For patients and families dealing with DRPLA or with a history of the disorder, this test provides a valuable tool for making informed decisions about their health and managing the condition effectively.
The Factor V Leiden Mutation Analysis Test is a specialized diagnostic procedure aimed at detecting the presence of the Factor V Leiden mutation in the DNA. This genetic mutation is associated with an increased risk of developing abnormal blood clots, which can lead to conditions such as deep vein thrombosis (DVT) or pulmonary embolism. The test involves analyzing a sample of the patient's blood to identify the specific mutation in the Factor V gene that is responsible for the altered function of the clotting factor.
At DNA Labs UAE, this crucial test is offered at a cost of 1290 AED. The laboratory utilizes advanced genetic testing technologies to ensure accurate and reliable results, providing essential information for the assessment of thrombophilia risk. By identifying individuals who carry the Factor V Leiden mutation, healthcare providers can make informed decisions regarding the need for preventive measures or treatment strategies to reduce the risk of thrombotic events. This test is an important tool in the management of patients with a personal or family history of clotting disorders, helping to tailor personalized healthcare plans and improve patient outcomes.
The "FISH - Amnio Two Probes Trisomy 13 and 21 Test" is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect chromosomal abnormalities, specifically Trisomy 13 (Patau syndrome) and Trisomy 21 (Down syndrome), in a fetus. This test utilizes Fluorescence In Situ Hybridization (FISH) technology, which involves using fluorescent probes to visualize and map out genes or chromosomes in cells extracted from amniotic fluid samples. This method allows for a rapid and accurate detection of the presence of an extra chromosome 13 or 21, which are the hallmarks of Trisomy 13 and Trisomy 21, respectively.
The test is particularly recommended for pregnant women who are at an increased risk of carrying a baby with these genetic disorders, either due to maternal age, family history, or abnormal results from other prenatal screenings. Conducted at DNA Labs UAE, a leading facility in genetic testing, the "FISH - Amnio Two Probes Trisomy 13 and 21 Test" ensures high accuracy and reliability, providing crucial information for expecting parents and their healthcare providers.
The cost of the test is set at 1290 AED, making it a valuable option for those seeking early and precise diagnosis of these chromosomal abnormalities. With this test, families can gain essential insights into their unborn child's health, allowing for informed decision-making regarding pregnancy management and preparation for any necessary medical interventions or support services after birth.
The "Rabies Viral RNA Detection Qualitative Test" is a specialized diagnostic procedure designed to identify the presence of rabies virus RNA in a sample. This test is crucial for confirming rabies infections, a deadly virus that affects the central nervous system of mammals, including humans. The test employs sophisticated molecular techniques to qualitatively detect rabies viral RNA, offering a high degree of sensitivity and specificity. Conducted at DNA Labs UAE, a leading facility in medical diagnostics, this test provides reliable results that are essential for timely and appropriate medical intervention. The cost of the test is 1200 AED, reflecting the advanced technology and expertise required to perform this critical diagnostic service.
The FISH (Fluorescence In Situ Hybridization) test for Trisomy 13, also known as Patau Syndrome, is a specialized diagnostic procedure available at DNA Labs UAE. Priced at 1200 AED, this test is designed to detect the presence of an extra chromosome 13, which is the hallmark of Patau Syndrome. This condition is associated with severe intellectual disability and physical abnormalities in newborns. The FISH technique involves using fluorescent probes that bind to specific parts of chromosomes, making it possible to visualize and identify chromosomal abnormalities with a high degree of accuracy. This test is crucial for early diagnosis, allowing for appropriate medical intervention and support for affected families. DNA Labs UAE employs state-of-the-art technology and expert technicians to ensure reliable and timely results for this important genetic test.
The FISH (Fluorescence In Situ Hybridization) test for Trisomy 18, also known as Edward Syndrome, is a specialized diagnostic procedure available at DNA Labs UAE. This test is designed to detect the presence of an extra chromosome 18, which is the hallmark of Edward Syndrome, a condition that leads to severe developmental and health issues in affected infants. The FISH technique involves using fluorescent probes that bind to specific parts of chromosomes, making it possible to visualize and count the number of chromosome 18s in a sample. This method provides a rapid and accurate diagnosis, which is crucial for early intervention and management of the condition. The test is priced at 1200 AED, offering families and healthcare providers in the UAE access to advanced genetic testing services for critical early detection of Trisomy 18.
The "FISH for X and Y Test" is a sophisticated diagnostic procedure offered by DNA Labs UAE, designed to identify chromosomal abnormalities related to the X and Y chromosomes. Standing for Fluorescence In Situ Hybridization, the FISH technique is a powerful tool that allows scientists to visualize and map out genetic material within individual cells. This test is particularly useful for assessing genetic disorders, sex chromosome anomalies, and for providing essential information in fertility assessments, prenatal diagnostics, and in the study of specific cancers.
At DNA Labs UAE, the FISH for X and Y Test is conducted with precision and care, utilizing state-of-the-art technology to ensure accurate and reliable results. The test is priced at 1200 AED, reflecting the advanced nature of the technology and the expertise required to perform it. This test is an invaluable resource for individuals and families seeking insights into genetic conditions related to the sex chromosomes, offering a crucial step towards diagnosis, management, and treatment planning.
The C7 Complement Test is a specialized diagnostic procedure aimed at measuring the level of the C7 component within the complement system of the immune system. This test is critical for diagnosing and monitoring conditions associated with complement system deficiencies, such as certain autoimmune diseases, recurrent bacterial infections, and inherited complement deficiencies. The complement system plays a vital role in the body's immune response, aiding in the elimination of pathogens. A deficiency in the C7 component can lead to increased susceptibility to infections and can impact the effectiveness of the immune response.
In the UAE, the C7 Complement Test is available at DNA Labs UAE, a leading diagnostic facility known for its advanced testing services and accurate results. The cost of the test at DNA Labs UAE is 1200 AED. This facility ensures the provision of high-quality healthcare services with state-of-the-art laboratory equipment and a team of experienced professionals. Patients opting for this test at DNA Labs UAE can expect reliable results, which are crucial for the appropriate management and treatment of conditions related to complement system deficiencies.
The C8 Complement Test is a specialized diagnostic procedure aimed at measuring the levels of the eighth component of the complement system (C8) in the blood. This test plays a crucial role in assessing the functionality and integrity of the complement system, which is an essential part of the body's immune defense mechanism against infections and in the process of inflammation. Abnormal levels of C8 can indicate issues related to the immune system, including autoimmune diseases, recurrent bacterial infections, and can sometimes point towards inherited complement deficiencies.
Performed at DNA Labs UAE, a leading facility in medical diagnostics, the test offers accurate and reliable results, contributing to the effective management and diagnosis of related health conditions. The cost of the C8 Complement Test at DNA Labs UAE is 1350 AED. The test is conducted under stringent quality controls and is interpreted by qualified professionals, ensuring patients receive comprehensive insights into their complement system's status. This aids healthcare providers in devising appropriate treatment strategies, ensuring a better health outcome for the patient.
