The Ganciclovir Resistance Detection Test is a specialized diagnostic procedure aimed at identifying resistance to ganciclovir, an antiviral medication primarily used for the treatment of cytomegalovirus (CMV) infections. This test is particularly crucial for patients who are undergoing antiviral therapy and exhibit a poor response to treatment, suggesting the possibility of a resistant viral strain. By analyzing the viral DNA, the test detects specific mutations in the CMV genome that are known to confer resistance to ganciclovir.
Conducted at DNA Labs UAE, a leading facility in genetic and molecular diagnostics, the test employs advanced molecular techniques to ensure accurate and reliable results. The cost of the Ganciclovir Resistance Detection Test is set at 1300 AED. The price reflects the sophisticated technology and expertise required to perform this specialized analysis. For patients and healthcare providers, the test offers valuable insights into treatment options, allowing for the adjustment of antiviral therapy to combat resistant CMV infections effectively.
The Felbamate Test is a specialized diagnostic procedure designed to monitor the levels of felbamate, an anticonvulsant medication used in the treatment of epilepsy, in a patient's bloodstream. This test is particularly crucial for individuals who are on felbamate therapy as it helps in ensuring the drug concentration stays within a therapeutic range, minimizing the risk of side effects while optimizing its effectiveness. Given the critical balance required in managing epilepsy treatment, the Felbamate Test is an essential tool for healthcare providers to tailor medication dosages to individual patient needs.
DNA Labs UAE, a leading diagnostic and analytical facility, offers the Felbamate Test for patients and healthcare professionals. The test cost is set at 1800 AED, reflecting the specialized nature of the test and the sophisticated technology employed in its execution. At DNA Labs UAE, patients can expect a seamless testing process, characterized by professional handling and accurate, timely results, all conducted in a state-of-the-art laboratory environment. This test is a testament to DNA Labs UAE's commitment to providing advanced healthcare solutions and supporting the management of chronic conditions like epilepsy with precision and care.
The "FISH - Amnio Three Probes Trisomy 18 X and Y Test" is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting specific chromosomal abnormalities in a fetus. This test employs Fluorescence In Situ Hybridization (FISH) technology to identify the presence of Trisomy 18 (Edwards syndrome) as well as abnormalities in the sex chromosomes (X and Y). Trisomy 18 is a condition where an individual has an extra copy of chromosome 18, leading to various developmental and health issues. Additionally, the test examines the X and Y chromosomes to detect potential disorders related to the sex chromosomes, such as Turner syndrome or Klinefelter syndrome.
Performed on amniotic fluid samples, this test provides rapid and accurate results, helping expectant parents and healthcare providers make informed decisions regarding the pregnancy. The cost of the "FISH - Amnio Three Probes Trisomy 18 X and Y Test" at DNA Labs UAE is 1760 AED. This test is crucial for early detection and intervention, potentially guiding the management of pregnancies at risk for these specific chromosomal abnormalities.
The IgVH Mutation Detection Screening Test is a sophisticated diagnostic procedure designed to identify mutations in the immunoglobulin heavy chain variable region (IgVH) gene. This gene plays a crucial role in the adaptive immune response, and mutations within it can be indicative of various hematological malignancies, including chronic lymphocytic leukemia (CLL). The presence or absence of these mutations provides valuable prognostic information, helping clinicians to predict disease progression and tailor treatment strategies accordingly.
Conducted at DNA Labs UAE, a leading facility in genetic testing and analysis, this test offers precise and reliable results. The cost of the IgVH Mutation Detection Screening Test is set at 1760 AED, reflecting the intricate technology and expertise required to accurately identify these genetic variations. By opting for this test at DNA Labs UAE, patients and healthcare providers can expect a high level of accuracy, comprehensive support, and detailed insights that are crucial for effective disease management and treatment planning.
The KRAS Mutation Codon 12 and 13 Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to detect mutations in codons 12 and 13 of the KRAS gene. These mutations are significant because they can influence the behavior of cancer cells, particularly in colorectal, lung, and pancreatic cancers. Identifying the presence of these mutations can be crucial for determining the most effective treatment plan for patients, as certain therapies may be more effective with specific genetic profiles.
This test involves analyzing the patient's DNA to look for specific alterations in the KRAS gene that could drive cancer progression or influence treatment response. The cost of the KRAS Mutation Codon 12 and 13 Test at DNA Labs UAE is 1760 AED, reflecting the sophisticated technology and expertise required to accurately identify these genetic changes. By providing this testing service, DNA Labs UAE plays a critical role in personalized cancer treatment, enabling healthcare providers to tailor their approaches based on the genetic makeup of an individual's cancer.
The "Neuroviruses Comprehensive Panel Qualitative PCR Test" is a sophisticated diagnostic tool offered by DNA Labs UAE, designed to detect a wide array of viruses that affect the nervous system. Utilizing the Polymerase Chain Reaction (PCR) technique, this test amplifies small segments of DNA or RNA from the virus, allowing for the rapid and accurate identification of various neurotropic viruses. These viruses can include, but are not limited to, herpes simplex virus, enteroviruses, and West Nile virus, all of which can cause severe neurological diseases ranging from meningitis to encephalitis.
The qualitative nature of the test means it is used to determine the presence or absence of these viruses' genetic material in a patient's sample, rather than quantifying the amount of virus present. This is crucial for early diagnosis and the initiation of appropriate treatment strategies to mitigate potential complications associated with these infections.
Conducted in the state-of-the-art facilities of DNA Labs UAE, the test is priced at 1760 AED. This cost reflects the comprehensive nature of the panel and the advanced technology employed to ensure accurate and reliable results. Patients looking for a thorough evaluation of potential neuroviral infections can opt for this test, with the assurance of receiving high-quality diagnostic services from a reputable laboratory.
The "SCA Spinocerebellar Ataxia Profile Any 4 Markers Test" is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify specific genetic markers associated with Spinocerebellar Ataxia (SCA). Spinocerebellar Ataxia is a term for a group of hereditary ataxias that are characterized by degenerative changes in the part of the brain related to the control of movement, and in some cases, other parts of the nervous system. These disorders are known for causing progressive problems with movement, coordination, and balance.
The test targets any 4 specific genetic markers out of the many known to be associated with different types of SCA, providing a tailored approach to diagnosing this complex group of disorders. Identifying the precise genetic cause of SCA in a patient can aid in determining the specific subtype of the disease, which is crucial for understanding the likely course of the condition, potential treatment options, and genetic counseling for the patient and their family.
The cost of the "SCA Spinocerebellar Ataxia Profile Any 4 Markers Test" at DNA Labs UAE is 1760 AED. This cost reflects the sophisticated technology and expertise required to accurately identify the genetic mutations associated with SCA. By opting for this test, patients and healthcare providers can gain valuable insights into the genetic underpinnings of Spinocerebellar Ataxia, facilitating more personalized and effective management of the condition.
The Fanconi's Anemia Stress Cytogenetics Test is a specialized diagnostic procedure aimed at identifying Fanconi Anemia (FA), a rare genetic disorder that affects the bone marrow and results in decreased production of all types of blood cells. This test is particularly important because individuals with FA have a higher risk of developing leukemia and other cancers. The test involves examining the chromosomes in a sample of the patient's blood cells under conditions that induce stress, as cells from individuals with Fanconi Anemia typically show increased chromosomal breakage when exposed to certain chemicals or radiation. This characteristic response helps in the diagnosis of FA.
At DNA Labs UAE, the Fanconi's Anemia Stress Cytogenetics Test is offered for 1760 AED. The lab utilizes state-of-the-art technology and follows stringent protocols to ensure accurate and reliable results. Given the complexity of the test and the critical information it provides, it represents a valuable tool for the early detection and management of Fanconi Anemia, thereby facilitating timely intervention and better patient outcomes.
The "JAK2 V617F Reflex to JAK2 Exon 12 Mutation Detection Test" is a specialized genetic test offered by DNA Labs UAE, designed to identify mutations associated with certain blood disorders, including myeloproliferative neoplasms (MPNs). This test first screens for the JAK2 V617F mutation, a common genetic alteration found in various types of MPNs. If the V617F mutation is not detected, the test then reflexes to search for mutations in exon 12 of the JAK2 gene, which could indicate other forms of MPNs.
This two-step approach ensures a comprehensive analysis for patients suspected of having MPNs, aiding in accurate diagnosis and treatment planning. The test cost is 1730 AED, reflecting the intricate technology and expertise required to perform this genetic analysis. By offering this test, DNA Labs UAE provides essential support in the diagnosis and management of blood disorders, contributing to improved patient outcomes.
The "Chlamydia Pneumonia Bacterial Load Test" is a diagnostic procedure aimed at detecting and quantifying the presence of Chlamydia pneumoniae bacteria in the body. This bacterium is a common cause of pneumonia and other respiratory tract infections, which can range from mild to severe. The test is particularly useful for patients exhibiting symptoms of respiratory infections or for those who are at a high risk of complications due to underlying health conditions.
Performed at DNA Labs UAE, a leading laboratory known for its advanced diagnostic solutions, the test involves collecting a sample from the patient, typically a throat swab or a sputum sample. This sample is then analyzed using sophisticated molecular techniques to identify the presence of Chlamydia pneumoniae DNA, thereby confirming infection. Moreover, the test quantifies the bacterial load, providing valuable information on the severity of the infection, which can guide treatment decisions.
The cost of the Chlamydia Pneumonia Bacterial Load Test at DNA Labs UAE is set at 1730 AED. While the price may seem high, it reflects the advanced technology and expertise required to accurately diagnose and quantify the bacterial infection. For patients and healthcare providers, this test offers a reliable means of identifying Chlamydia pneumoniae infections, enabling timely and appropriate treatment interventions.
