The "CAV3 Gene Creatine Phosphokinase Elevated Serum Genetic Test" is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the CAV3 gene, which can lead to elevated levels of creatine phosphokinase (CPK) in the serum. This enzyme is crucial for energy production in muscle cells, and its elevated levels can indicate muscle damage or certain genetic conditions, such as muscular dystrophies. The test, priced at 4400 AED, involves analyzing the patient's DNA to detect any genetic variations in the CAV3 gene that might contribute to the abnormal enzyme levels. This information can be invaluable for diagnosing underlying conditions, guiding treatment decisions, and assessing the risk of passing the condition to future generations.
The PRNP Gene Creutzfeldt-Jakob Disease (CJD) Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the PRNP gene, which are linked to the development of Creutzfeldt-Jakob Disease, a rare and fatal degenerative brain disorder. This test is crucial for individuals with a family history of CJD or those exhibiting symptoms of the disease, as it can confirm the genetic predisposition and assist in the early diagnosis and management of the condition. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test provides a comprehensive analysis of the PRNP gene to detect specific mutations associated with CJD. The cost of the test is 4400 AED, reflecting the intricate technology and expertise required to accurately identify the genetic variations linked to this devastating disease.
The MT-CO1 gene, encoding for Cytochrome C Oxidase 1, plays a critical role in the mitochondrial respiratory chain, which is essential for energy production in cells. Deficiencies in this gene can lead to a range of mitochondrial disorders, characterized by symptoms such as muscle weakness, heart problems, and neurological issues. Early diagnosis through genetic testing is crucial for managing these conditions.
The MT-CO1 Gene Cytochrome C Oxidase 1 Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the MT-CO1 gene. This test is pivotal for individuals exhibiting symptoms of mitochondrial disorders or those with a family history of such conditions, as it can provide definitive diagnosis and guide treatment options.
The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for any genetic abnormalities in the MT-CO1 gene. The process is highly accurate and provides vital information for the management of the associated conditions.
The cost of the MT-CO1 Gene Cytochrome C Oxidase 1 Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This investment can be crucial for individuals seeking insights into their genetic health, potentially leading to early intervention and better management of mitochondrial disorders.
The MT-CO2 Gene Cytochrome C Oxidase 2 Deficiency Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the MT-CO2 gene. This gene is crucial for the proper functioning of cytochrome c oxidase, an essential component of the mitochondrial respiratory chain responsible for cellular energy production. Deficiencies in cytochrome c oxidase can lead to a variety of mitochondrial disorders, which may present as muscle weakness, heart problems, and neurological issues, among other symptoms.
The test is particularly valuable for individuals presenting symptoms suggestive of mitochondrial disorders, those with a family history of such conditions, or for the purpose of confirming a clinical diagnosis through genetic analysis. By analyzing the genetic makeup of an individual, the test can detect specific mutations in the MT-CO2 gene that are known to cause cytochrome c oxidase deficiency, thereby aiding in the diagnosis, management, and understanding of the patient's condition.
Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, the test is priced at 4400 AED. This cost reflects the sophisticated nature of the testing process, which involves detailed genetic analysis and interpretation by specialized professionals. Patients undergoing this test can expect a comprehensive assessment of their genetic risk, contributing to more informed healthcare decisions and personalized treatment plans.
The MT-CO3 gene is responsible for encoding a crucial subunit of cytochrome c oxidase, which is part of the mitochondrial respiratory chain complex IV. This enzyme complex plays a vital role in the process of oxidative phosphorylation, where cells produce ATP, the primary energy currency of the cell. Mutations or deficiencies in the MT-CO3 gene can disrupt this process, leading to a variety of mitochondrial disorders that can affect multiple systems in the body, particularly those with high energy demands such as the nervous system and muscles.
The Cytochrome C Oxidase 3 Deficiency Genetic Test is a specialized diagnostic tool designed to identify mutations in the MT-CO3 gene. This test is crucial for individuals who exhibit symptoms suggestive of mitochondrial disorders, including muscle weakness, neurological deficits, and heart problems, among others. Early and accurate diagnosis through this genetic testing can aid in the management of the condition, allowing for targeted treatments and interventions that can improve quality of life and outcomes for affected individuals.
The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. DNA Labs UAE employs state-of-the-art technology and expertise to deliver accurate and reliable genetic testing results. The cost of the Cytochrome C Oxidase 3 Deficiency Genetic Test is 4400 AED, reflecting the comprehensive analysis and the specialized nature of the test. This investment can be invaluable for families seeking answers to complex health issues related to mitochondrial dysfunction and offers a pathway towards personalized medical care based on genetic insights.
The LAMP2 Gene Danon Disease Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the LAMP2 gene, which are responsible for Danon Disease. Danon Disease is a rare genetic disorder characterized by weakening of the heart muscle (cardiomyopathy), muscle weakness, and intellectual disability. The condition is inherited in an X-linked dominant manner, meaning it can affect both males and females, but tends to have more severe effects in males.
This genetic test involves analyzing the patient's DNA to identify mutations in the LAMP2 gene, which provides instructions for making a protein found in lysosomes - essential components of cells that break down waste materials. Mutations in this gene disrupt the normal functioning of lysosomes, leading to the accumulation of waste products in cells, which contributes to the symptoms of Danon Disease.
At DNA Labs UAE, the LAMP2 Gene Danon Disease Genetic Test is meticulously conducted to ensure accurate diagnosis, which is crucial for the management and treatment of the condition. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to perform this genetic analysis. Early diagnosis through this test can significantly impact the management of Danon Disease, offering affected individuals and their families a better understanding of the condition and guidance on managing symptoms and potential treatments.
The EGR2 Gene Dejerine-Sottas Disease Genetic Test is a specialized diagnostic examination available at DNA Labs UAE, designed to identify mutations in the EGR2 gene, which are linked to the development of Dejerine-Sottas Disease (DSD). DSD, also known as hereditary motor and sensory neuropathy type III, is a rare genetic disorder characterized by severe demyelination of peripheral nerves, leading to muscle weakness, sensory loss, and in some cases, deformities of the extremities.
This test plays a crucial role in the early detection and management of the disease, allowing for a tailored approach to treatment and care for affected individuals. The process involves collecting a DNA sample, typically through a blood draw, which is then analyzed for specific genetic alterations in the EGR2 gene that are associated with the condition.
At DNA Labs UAE, the EGR2 Gene Dejerine-Sottas Disease Genetic Test is priced at 4400 AED. The cost reflects the sophisticated technology and expertise required to accurately identify the genetic variations linked to this rare condition. By opting for this test, patients and their families can gain valuable insights into the genetic basis of the disease, facilitating informed decisions about management and therapy options.
The GJB1 Gene Dejerine-Sottas Disease Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the GJB1 gene, which are associated with Dejerine-Sottas Disease (DSD), also known as hereditary motor and sensory neuropathy type III. This condition is characterized by progressive nerve damage leading to muscle weakness, decreased sensation, and other neurological symptoms. The test is crucial for confirming the diagnosis, understanding the disease's progression, and guiding treatment decisions.
Performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test involves collecting a DNA sample, typically through a blood draw or cheek swab. The laboratory then analyzes the GJB1 gene for specific mutations that contribute to the development of Dejerine-Sottas Disease.
The cost of the GJB1 Gene Dejerine-Sottas Disease Genetic Test at DNA Labs UAE is 4400 AED. This price may cover the genetic analysis, professional interpretation of results, and post-test counseling to discuss the findings and their implications. Patients considering this test should consult with their healthcare provider to understand its benefits, potential limitations, and how the results might influence their treatment plan.
The MPZ Gene Dejerine-Sottas Disease Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the MPZ gene associated with Dejerine-Sottas Disease (DSD), also known as hereditary motor and sensory neuropathy type III. DSD is a rare genetic disorder characterized by progressive nerve damage leading to muscle weakness, sensory loss, and in severe cases, disability. The MPZ gene plays a crucial role in the development and function of myelin, the protective sheath surrounding nerve fibers, and mutations in this gene can disrupt nerve signal transmission.
This genetic test involves analyzing the patient's DNA to detect specific mutations in the MPZ gene that are linked to the development of Dejerine-Sottas Disease. Early diagnosis through this test can be crucial for managing symptoms, implementing appropriate therapies, and providing genetic counseling for affected families.
The test is priced at 4400 AED and is conducted at DNA Labs UAE, which is equipped with state-of-the-art technology and staffed by experienced professionals to ensure accurate and reliable results. Individuals undergoing this test can expect a comprehensive analysis, with results that can guide treatment decisions and offer insights into the hereditary nature of the condition.
The PMP22 Gene Dejerine-Sottas Disease Genetic Test is a specialized diagnostic tool used to detect mutations in the PMP22 gene, which are associated with Dejerine-Sottas Disease, also known as hereditary motor and sensory neuropathy type III. This condition is a type of Charcot-Marie-Tooth disease, characterized by severe neurological symptoms that include muscle weakness, sensory loss, and in some cases, deformities in the extremities due to nerve damage.
DNA Labs UAE offers this genetic test to individuals who exhibit symptoms of Dejerine-Sottas Disease or have a family history of the condition. The test involves collecting a DNA sample, usually through a blood draw, which is then analyzed in the lab to identify any mutations in the PMP22 gene.
The cost of the PMP22 Gene Dejerine-Sottas Disease Genetic Test at DNA Labs UAE is 4400 AED. This price may cover the test procedure, analysis, and a comprehensive report that explains the results. It's important for patients to consult with a healthcare provider or a genetic counselor before and after taking the test to understand the implications of the results and to discuss potential treatment options or management strategies for the condition.
