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-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.
The PRX Gene CMT4F Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the PRX gene, which are known to cause Charcot-Marie-Tooth disease type 4F (CMT4F). Charcot-Marie-Tooth disease is a group of inherited disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems, primarily in the arms and legs. CMT4F is a rare subtype characterized by severe nerve damage and onset in childhood or adolescence.
This genetic test involves analyzing the patient's DNA to search for specific alterations in the PRX gene that are indicative of CMT4F. Early detection through this test can be crucial for the management and treatment of the condition, allowing healthcare providers to tailor interventions that can help manage symptoms, improve quality of life, and provide genetic counseling for affected families.
The cost of the PRX Gene CMT4F Genetic Test at DNA Labs UAE is 4400 AED. The test is conducted in a state-of-the-art laboratory setting by professionals who specialize in genetic diagnostics. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed using advanced genetic sequencing technologies to identify any mutations in the PRX gene.
Choosing DNA Labs UAE for this test ensures access to leading-edge technology, expert analysis, and comprehensive support throughout the testing process, making it a valuable resource for individuals and families seeking answers about Charcot-Marie-Tooth disease type 4F.
The FGD4 gene CMT4H genetic test is a specialized diagnostic tool used to detect mutations in the FGD4 gene, which are responsible for causing Charcot-Marie-Tooth disease type 4H (CMT4H). CMT4H is a rare form of Charcot-Marie-Tooth disease, a neurological disorder that leads to peripheral nerve damage. This condition typically manifests in early childhood and is characterized by muscle weakness, sensory loss, and potential deformities in the feet and hands.
The test is crucial for individuals showing symptoms of CMT4H or those with a family history of the condition, as it provides definitive genetic evidence of the disorder. Early diagnosis through genetic testing can aid in the management of symptoms and improve the quality of life for affected individuals.
Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The cost of the FGD4 gene CMT4H genetic test is 4400 AED. The test is conducted under stringent laboratory conditions by highly qualified professionals, ensuring that patients receive precise results for effective disease management and counseling.
The FIG4 Gene CMT4J Genetic Test is a specialized diagnostic tool designed to detect mutations in the FIG4 gene, which are linked to Charcot-Marie-Tooth disease type 4J (CMT4J). CMT4J is a rare and severe neurological disorder characterized by progressive weakness and atrophy of the muscles in the feet, hands, and elsewhere. The condition can also affect sensory nerves, leading to a loss of sensation in the affected areas.
This genetic test is crucial for individuals suspected of having CMT4J based on clinical symptoms or family history. Early and accurate diagnosis through the FIG4 Gene CMT4J Genetic Test allows for better management of the condition, including therapeutic interventions and genetic counseling for affected families.
The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED. DNA Labs UAE utilizes state-of-the-art technology and adheres to the highest standards of accuracy and reliability in genetic diagnostics, ensuring that individuals receive comprehensive and precise information about their genetic health.
