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 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.
The TMEM70 gene plays a critical role in the proper function of mitochondrial complex V, also known as ATP synthase, which is essential for energy production within cells. Mutations in the TMEM70 gene can lead to a rare disorder known as mitochondrial complex V ATP synthase deficiency nuclear type 2. This condition is characterized by a wide range of symptoms, including metabolic acidosis, hypotonia, and developmental delay, due to the inefficient production of ATP, the primary energy carrier in cells.
To diagnose this condition, genetic testing is crucial. DNA Labs UAE offers a specific test targeting the TMEM70 gene to identify mutations that may lead to mitochondrial complex V ATP synthase deficiency nuclear type 2. The test is a comprehensive analysis of the TMEM70 gene to detect any genetic abnormalities that could impair the function of the ATP synthase complex.
The cost of the test is 4400 AED. This investment covers the process of collecting a DNA sample, usually through a blood draw or cheek swab, and the subsequent laboratory analysis to identify any mutations in the TMEM70 gene. The results from this test can provide essential information for the diagnosis, and potentially the management, of the condition. It is a crucial step for families seeking answers to unexplained symptoms related to energy metabolism disorders.
The ATP5F1E Gene Mitochondrial Complex V ATP Synthase Deficiency Nuclear Type 3 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the ATP5F1E gene. This gene plays a crucial role in the functioning of mitochondrial complex V, also known as ATP synthase, which is essential for the production of ATP, the main energy currency of the cell. Mutations in the ATP5F1E gene can lead to mitochondrial complex V deficiency, a condition that can affect various bodily systems and lead to a range of clinical symptoms, including neurological disorders, muscle weakness, and heart problems.
This genetic test is performed at DNA Labs UAE, a leading facility in genetic diagnostics, offering a comprehensive range of genetic testing services. The test involves collecting a DNA sample, typically through a blood draw, and then analyzing the genetic material for specific mutations in the ATP5F1E gene that are known to cause mitochondrial complex V ATP synthase deficiency nuclear type 3.
The cost of the ATP5F1E Gene Mitochondrial Complex V ATP Synthase Deficiency Nuclear Type 3 Genetic Test is 4400 AED. The test is designed for individuals who are experiencing symptoms suggestive of mitochondrial disorders, or who have a family history of such conditions, providing them with crucial information for diagnosis, treatment planning, and understanding their risk of passing the condition on to their offspring.
The ATP5F1A Gene Mitochondrial Complex V Deficiency Nuclear Type 4 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE. This test is designed to identify mutations in the ATP5F1A gene, which are implicated in Mitochondrial Complex V Deficiency, Nuclear Type 4. This condition is a rare genetic disorder that affects the body's ability to produce energy at the cellular level, leading to a range of symptoms that can include muscle weakness, neurological deficits, and developmental delays.
Mitochondrial Complex V, also known as ATP synthase, plays a crucial role in the final step of oxidative phosphorylation, where the majority of cellular ATP, the energy currency of the cell, is produced. Mutations in the ATP5F1A gene can impair the function of Complex V, resulting in reduced ATP production and the aforementioned symptoms.
The genetic test conducted at DNA Labs UAE involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific mutations in the ATP5F1A gene. This test is crucial for the accurate diagnosis of Mitochondrial Complex V Deficiency, Nuclear Type 4, and can provide essential information for managing the condition, including potential treatments and understanding the risk of passing the mutation to offspring.
The cost of the ATP5F1A Gene Mitochondrial Complex V Deficiency Nuclear Type 4 Genetic Test at DNA Labs UAE is 4400 AED. Given the complexity of the test and the specialized technology and expertise required to perform it, the cost reflects the comprehensive analysis and detailed report provided to patients and their healthcare providers. This test is a valuable tool for individuals and families seeking answers to unexplained symptoms related to energy metabolism disorders.
