The ACTA2 gene multisystemic smooth muscle dysfunction syndrome genetic test is a specialized diagnostic tool used to identify mutations in the ACTA2 gene, which can lead to a range of health issues affecting the smooth muscles throughout the body. This condition, known as multisystemic smooth muscle dysfunction syndrome, can manifest in various forms, including vascular disease, lung problems, and urinary tract issues, among others. Early detection through this genetic test can be crucial for managing symptoms and preventing severe complications.
The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the test is 4400 AED, an investment in health that provides individuals and families with vital information for managing the condition and planning for the future. DNA Labs UAE utilizes state-of-the-art technology to ensure accurate and reliable results, offering a comprehensive analysis of the ACTA2 gene for any mutations that may be present.
The MSTN Gene Muscle Hypertrophy Genetic Test, available at DNA Labs UAE for 3200 AED, is a cutting-edge diagnostic tool designed to analyze the myostatin (MSTN) gene, which plays a critical role in regulating muscle growth. Myostatin is a protein that inhibits muscle growth, and variations in the MSTN gene can lead to reduced myostatin activity, resulting in increased muscle mass and strength, a condition known as muscle hypertrophy. This test is particularly relevant for athletes, fitness enthusiasts, and individuals interested in understanding their genetic predisposition to muscle development. By identifying specific genetic markers, the test can provide insights into one's potential for muscle growth, enabling tailored training and nutrition programs. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test ensures confidentiality, accuracy, and comprehensive analysis, making it a valuable tool for those aiming to optimize their physical performance and body composition based on their genetic blueprint.
The POMK gene is associated with a rare genetic disorder known as Muscle-Eye-Brain Disease (MEB), which is characterized by muscle weakness, structural eye defects, and brain abnormalities. Mutations in the POMK gene disrupt the normal development of these organs, leading to the symptoms observed in individuals with MEB. The POMK-related genetic test is a specialized diagnostic tool designed to identify mutations in the POMK gene, providing crucial information for the diagnosis and management of Muscle-Eye-Brain Disease.
Performed at DNA Labs UAE, the test involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of mutations in the POMK gene. This genetic testing is vital for confirming the diagnosis of MEB, understanding the risk of passing the condition to future generations, and guiding treatment and management decisions.
The cost of the POMK-related genetic test at DNA Labs UAE is 4400 AED. This cost covers the full process of the genetic analysis, from sample collection to the provision of a detailed report explaining the test results. It's important for patients to consult with their healthcare provider to understand the implications of the test results and the best course of action following diagnosis.
The LAMA2 gene muscular dystrophy Type 1A genetic test is a specialized diagnostic procedure aimed at detecting mutations in the LAMA2 gene, which are indicative of Muscular Dystrophy Type 1A, also known as Merosin-deficient congenital muscular dystrophy. This condition is characterized by muscle weakness and wasting, primarily affecting the voluntary muscles used for activities such as crawling and walking. Early detection through genetic testing is crucial for managing symptoms, planning treatment strategies, and providing genetic counseling for affected families.
Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific mutations in the LAMA2 gene. The presence of these mutations can confirm a diagnosis of Muscular Dystrophy Type 1A, enabling healthcare providers to tailor interventions more effectively and offer support to families dealing with the implications of this genetic condition.
The cost of the LAMA2 gene muscular dystrophy Type 1A genetic test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of obtaining a definitive diagnosis and the potential to significantly impact the patient's treatment plan and quality of life can be invaluable. Patients considering this test are encouraged to discuss it with their healthcare provider to fully understand its benefits and implications.
The FKRP gene muscular dystrophy type 1C genetic test is a specialized diagnostic procedure aimed at identifying mutations in the FKRP gene, which are known to cause a form of limb-girdle muscular dystrophy (LGMD1C). This condition is characterized by progressive weakness and wasting of the muscles around the hips and shoulders, affecting mobility and physical capabilities over time. The test involves analyzing the patient's DNA to pinpoint any genetic abnormalities in the FKRP gene, which plays a crucial role in muscle function and integrity.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test is priced at 4400 AED. This cost encompasses the full process of sample collection, genetic sequencing, and expert analysis to ensure accurate identification of any mutations associated with the condition. The results from this test are critical for confirming a diagnosis of LGMD1C, which can then guide treatment options and genetic counseling for affected individuals and their families. This genetic test is a key step towards personalized care, offering insights into the specific genetic alterations driving the disease and enabling targeted management strategies.
The LARGE1 Gene Muscular Dystrophy Type 1D Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the LARGE1 gene, which are associated with Muscular Dystrophy Type 1D (MD1D). This condition is a rare form of muscular dystrophy that affects muscle function and strength, leading to progressive muscle weakness. The test is crucial for accurate diagnosis, allowing for appropriate management and treatment strategies to be implemented for affected individuals.
Performed at DNA Labs UAE, a leading facility in genetic testing, this test offers a comprehensive analysis of the LARGE1 gene to detect any genetic anomalies that may contribute to MD1D. The process involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed using advanced genetic sequencing technologies to identify mutations in the LARGE1 gene.
The cost of the LARGE1 Gene Muscular Dystrophy Type 1D Genetic Test is 4400 AED. This price includes the cost of the sample collection, genetic analysis, and a detailed report of the findings. The report not only provides information on the presence of any genetic mutations associated with MD1D but also offers insights into the implications of these mutations for the patient and potential family members.
Given the genetic nature of Muscular Dystrophy Type 1D, this test is particularly valuable for individuals with a family history of the condition or those exhibiting symptoms related to muscular dystrophies. Early and accurate diagnosis through genetic testing can significantly impact the management of the condition, including tailored treatment plans and genetic counseling for families.
The "DMD Gene Muscular Dystrophy Becker Type Genetic Test" is a specific diagnostic tool used to identify mutations in the DMD gene, which are responsible for Becker Muscular Dystrophy (BMD). This condition is a milder form of muscular dystrophy that primarily affects males, leading to muscle weakness and degeneration over time. Unlike its more severe counterpart, Duchenne Muscular Dystrophy, individuals with Becker Muscular Dystrophy tend to experience symptoms later in childhood or in adolescence, and the progression of the disease is generally slower.
The test is conducted at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services. By analyzing a sample of the patient's DNA, the test can detect specific mutations in the DMD gene that are indicative of Becker Muscular Dystrophy. This information is crucial for confirming the diagnosis, understanding the severity of the condition, and informing treatment and management strategies.
The cost of the DMD Gene Muscular Dystrophy Becker Type Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of obtaining an accurate diagnosis and the potential to tailor treatment plans specifically to the genetic makeup of the individual can be invaluable for those affected by this condition.
The LMNA gene muscular dystrophy, also known as congenital LMNA-related muscular dystrophy, is a rare genetic disorder characterized by muscle weakness and wasting. This condition is caused by mutations in the LMNA gene, which provides instructions for making a protein that is essential for the structural integrity and function of cells in the body. Individuals affected by this condition may experience symptoms ranging from mild to severe, including muscle weakness, cardiac issues, and skeletal abnormalities.
To diagnose this condition, a genetic test is available at DNA Labs UAE, which specifically looks for mutations in the LMNA gene associated with muscular dystrophy. The test is a crucial step in confirming the diagnosis, understanding the severity of the condition, and guiding treatment and management decisions.
The cost of the LMNA-related genetic test at DNA Labs UAE is 4400 AED. This test is performed using a sample of the patient's blood or saliva, and it involves analyzing the DNA to identify any mutations in the LMNA gene. Results from this test can provide valuable information for affected individuals and their families regarding prognosis, potential interventions, and genetic counseling.
The "MT-ATP6 Gene Mitochondrial Complex V ATP Synthase Deficiency Genetic Test" is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the MT-ATP6 gene. This gene plays a critical role in the normal functioning of mitochondrial complex V, also known as ATP synthase. ATP synthase is essential for ATP production, the main energy currency in cells. Mutations in the MT-ATP6 gene can lead to mitochondrial disorders, which are complex and can affect multiple systems in the body, often with severe outcomes.
This test is particularly important for individuals showing symptoms suggestive of mitochondrial diseases or for those with a family history of such conditions. Early and accurate diagnosis through this genetic test can aid in the management of the disease, allowing for tailored treatments and interventions to improve quality of life.
The test is conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services. The cost of the test is 4400 AED, which reflects the sophisticated nature of the analysis and the invaluable insights it provides into the patient's genetic health, particularly concerning mitochondrial function.
The ATPAF2 gene plays a crucial role in the normal function and assembly of mitochondrial complex V, also known as ATP synthase. This enzyme complex is essential for ATP production, which is the primary energy currency in cells. Deficiencies in this complex can lead to a range of mitochondrial disorders, characterized by a wide spectrum of symptoms due to the fundamental role of ATP in cellular processes.
Mitochondrial complex V ATP synthase deficiency nuclear type 1 is a genetic condition caused by mutations in the ATPAF2 gene. This disorder can manifest in various clinical presentations, including neurological and muscular impairments, highlighting the importance of accurate diagnosis.
The genetic test for ATPAF2 gene mitochondrial complex V ATP synthase deficiency nuclear type 1 is a sophisticated diagnostic tool aimed at identifying mutations in the ATPAF2 gene. Performed at DNA Labs UAE, this test involves analyzing the patient's DNA to detect abnormalities in the ATPAF2 gene that may lead to the disease. The process helps in confirming the diagnosis, which is crucial for managing the condition effectively and providing appropriate genetic counseling.
The cost of the ATPAF2 gene mitochondrial complex V ATP synthase deficiency nuclear type 1 genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the genetic mutations associated with the condition, offering invaluable information for affected individuals and their families regarding the management and potential treatment options for this complex disorder.
