The MT-ND6 gene plays a crucial role in the mitochondrial complex I, which is essential for the mitochondrial respiratory chain. This chain is responsible for producing energy in cells. Mutations in the MT-ND6 gene can lead to mitochondrial complex I deficiency, a condition that affects various body systems, particularly the nervous system and muscles. Symptoms can range from muscle weakness and exercise intolerance to more severe neurodegenerative disorders.
To diagnose this condition, a genetic test targeting the MT-ND6 gene can be performed. This test looks for mutations in the MT-ND6 gene that are known to cause mitochondrial complex I deficiency. It is a critical step for confirming the diagnosis, understanding the disease's progression, and managing it effectively.
In the UAE, DNA Labs UAE offers this specific genetic test. The cost of the test is 4400 AED. Conducting the test at DNA Labs UAE ensures that patients receive accurate and reliable results, thanks to their state-of-the-art facilities and experienced genetic professionals. This test is crucial for patients suspected of having mitochondrial complex I deficiency, as it can guide treatment options and help in the management of symptoms.
The NDUFA1 Gene Mitochondrial Complex I Deficiency Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the NDUFA1 gene. These mutations can lead to mitochondrial complex I deficiency, a condition that affects mitochondrial function, resulting in a wide range of clinical manifestations, including neuromuscular disorders and systemic energy metabolism issues. Mitochondrial complex I is crucial for the electron transport chain, a key component in cellular energy production.
This genetic test is vital for individuals showing symptoms suggestive of mitochondrial disorders or for families with a history of such conditions, aiming to provide a definitive diagnosis. Understanding the genetic basis of the condition can help in tailoring management plans, potential treatments, and genetic counseling for affected families.
DNA Labs UAE offers this test at a cost of 4400 AED, utilizing cutting-edge genetic sequencing technologies to ensure accurate and reliable results. The test is conducted in a state-of-the-art laboratory setting, adhering to stringent quality controls, and is performed by a team of specialized geneticists and laboratory technicians.
The NDUFA11 gene plays a crucial role in the proper functioning of mitochondrial complex I, which is essential for energy production in cells. Mutations in the NDUFA11 gene can lead to mitochondrial complex I deficiency, a condition that can result in a wide range of clinical manifestations including neurological disorders, muscle weakness, and metabolic problems.
To diagnose this condition, a genetic test targeting the NDUFA11 gene can be performed. This test involves analyzing the DNA to identify mutations in the NDUFA11 gene that might be causing mitochondrial complex I deficiency.
In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost for the NDUFA11 Gene Mitochondrial Complex I Deficiency Genetic Test is 4400 AED. This test is crucial for individuals suspected of having mitochondrial complex I deficiency, as it can provide definitive diagnosis and guide treatment and management options.
The NDUFAF1 Gene Mitochondrial Complex I Deficiency Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the NDUFAF1 gene. These mutations are linked to mitochondrial complex I deficiency, a condition that affects mitochondrial function, leading to a range of symptoms including muscle weakness, heart problems, and neurological issues. The test, priced at 4400 AED, involves analyzing the patient's DNA to detect any abnormalities in the NDUFAF1 gene, which plays a crucial role in the assembly and function of mitochondrial complex I. By identifying these mutations, healthcare providers can better understand the condition, leading to more targeted treatments and management strategies for affected individuals.
The NDUFAF3 gene plays a crucial role in the mitochondrial complex I assembly, which is essential for the normal function of mitochondria, the energy-producing organelles in cells. Mutations in the NDUFAF3 gene can lead to mitochondrial complex I deficiency, a condition that affects the mitochondrial respiratory chain. This deficiency can result in a wide range of clinical manifestations, including muscle weakness, neurodegenerative disorders, and metabolic abnormalities, due to the impaired energy production in cells.
To diagnose this condition, a genetic test targeting the NDUFAF3 gene can be conducted. DNA Labs UAE offers this specific test, providing a vital tool for the diagnosis of mitochondrial complex I deficiency caused by NDUFAF3 mutations. The test involves analyzing the patient's DNA to identify mutations in the NDUFAF3 gene that are known to cause the disorder. This genetic testing is crucial for confirming the diagnosis, understanding the disease's progression, and guiding treatment options.
The cost of the NDUFAF3 gene mitochondrial complex I deficiency genetic test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect the presence of mutations in the NDUFAF3 gene. Given the specialized nature of this test and its importance in diagnosing a potentially severe and complex condition, the test is a critical step for patients exhibiting symptoms suggestive of mitochondrial complex I deficiency or for those with a family history of the condition.
The NDUFAF4 Gene Mitochondrial Complex I Deficiency Genetic Test is a specialized diagnostic examination aimed at detecting mutations in the NDUFAF4 gene, which is crucial for the normal functioning of mitochondrial complex I. Mitochondrial complex I is essential for energy production within cells, and deficiencies in this complex can lead to a range of severe mitochondrial disorders, affecting various bodily systems, particularly the nervous system and muscles.
This test is particularly important for individuals presenting symptoms of mitochondrial disorders, or for those with a family history of such conditions, as it can provide a definitive diagnosis. By analyzing the genetic makeup of an individual, this test identifies specific mutations in the NDUFAF4 gene that are known to cause mitochondrial complex I deficiency.
Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, the test ensures accuracy and reliability. The cost of the NDUFAF4 Gene Mitochondrial Complex I Deficiency Genetic Test is set at 4400 AED. This investment covers the comprehensive analysis required to detect the presence of genetic mutations associated with the condition, providing crucial information for the management and treatment of affected individuals. It represents a significant step forward in personalized medicine, offering hope and answers to those affected by mitochondrial disorders.
The NDUFAF5 gene plays a crucial role in the proper functioning of mitochondrial complex I, a vital component of the mitochondrial respiratory chain responsible for energy production in cells. Mutations in the NDUFAF5 gene can lead to mitochondrial complex I deficiency, a genetic disorder that affects various body systems, particularly the nervous system and muscles, leading to a wide range of health issues.
To diagnose this condition, a genetic test specifically targeting the NDUFAF5 gene can be conducted. This test is crucial for identifying mutations in the gene, confirming a diagnosis, and guiding treatment and management decisions. It involves collecting a DNA sample, typically through a blood draw, which is then analyzed in a laboratory for any genetic abnormalities associated with mitochondrial complex I deficiency.
In the UAE, DNA Labs UAE offers this specialized genetic test. The cost of the NDUFAF5 Gene Mitochondrial Complex I Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This state-of-the-art facility ensures accurate and reliable testing, employing the latest in genetic testing technology and methodologies. The test not only aids in the diagnosis but also plays a role in family planning and understanding the risk of recurrence in future pregnancies.
The NDUFB3 gene plays a crucial role in the proper functioning of mitochondrial complex I, a key component of the mitochondrial respiratory chain responsible for energy production in cells. Mutations in the NDUFB3 gene can lead to mitochondrial complex I deficiency, a genetic condition that can cause a wide range of clinical symptoms, including neuromuscular disorders and metabolic abnormalities.
To diagnose this condition, a genetic test is available at DNA Labs UAE, which specifically targets the NDUFB3 gene to identify mutations that may result in mitochondrial complex I deficiency. This test is essential for confirming the diagnosis, understanding the disease's progression, and guiding treatment options.
The cost of the NDUFB3 Gene Mitochondrial Complex I Deficiency Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to detect mutations in the NDUFB3 gene, providing crucial information for affected individuals and their families.
The "BRWD3 Gene Mental Retardation X-Linked Type 93 Genetic Test" is a specialized diagnostic tool offered by DNA Labs UAE, aimed at detecting mutations in the BRWD3 gene, which are associated with X-Linked Mental Retardation Type 93. This condition is a genetic disorder that primarily affects males, leading to various degrees of intellectual disability and possibly other physical or neurological symptoms. The test plays a crucial role in the early diagnosis and management of the condition, enabling healthcare providers to tailor interventions and support to the needs of the individual.
Performed through a blood sample or cheek swab, the test analyzes the DNA for specific mutations in the BRWD3 gene that are linked to the disorder. It is particularly recommended for families with a history of X-linked mental retardation or for individuals showing related symptoms without a clear diagnosis.
The cost of the test at DNA Labs UAE is 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive insights it provides into the individual's genetic makeup. This information can be invaluable for affected families, offering them a clearer understanding of their genetic conditions and guiding them towards appropriate therapeutic and supportive measures.
The GRIA3 Gene Mental Retardation X-Linked Type 94 Genetic Test is a specialized diagnostic tool designed to identify mutations in the GRIA3 gene, which have been associated with X-linked mental retardation type 94. This condition is a genetic disorder that primarily affects males and is characterized by various degrees of intellectual disability, developmental delays, and in some cases, physical abnormalities or behavioral issues. The GRIA3 gene plays a crucial role in the brain's communication pathways, and mutations in this gene can disrupt normal brain development and function.
This genetic test involves analyzing the DNA to detect any abnormalities in the GRIA3 gene that might indicate the presence of X-linked mental retardation type 94. It is a critical step for families seeking answers about developmental issues in their male children, as a positive identification of a mutation can help in understanding the condition better, planning for the future, and potentially connecting with therapies and support networks tailored to this specific type of intellectual disability.
The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expertise required to accurately identify mutations in the GRIA3 gene. Families considering this test can expect professional guidance, confidentiality, and support throughout the testing process at DNA Labs UAE, ensuring they receive the information needed to make informed decisions about their loved one's care and well-being.
