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ELAC2 Gene Combined oxidative phosphorylation deficiency type 17 Genetic Test Cost
The ELAC2 Gene Combined Oxidative Phosphorylation Deficiency Type 17 Genetic Test is a sophisticated diagnostic tool available at DNA Labs UAE, designed to identify mutations in the ELAC2 gene, which are linked to Combined Oxidative Phosphorylation Deficiency 17 (COXPD17). This condition is a rare genetic disorder that affects mitochondrial function, leading to a wide range of symptoms including developmental delay, muscle weakness, and in some cases, more severe organ dysfunction. The test, priced at 4400 AED, involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific genetic alterations in the ELAC2 gene. This test is crucial for early diagnosis and management of the condition, allowing healthcare providers to tailor treatments that can significantly improve the quality of life for affected individuals. DNA Labs UAE is equipped with state-of-the-art technology and staffed by genetic experts, ensuring accurate and reliable test results.
SFXN4 Gene Combined oxidative phosphorylation deficiency type 18 Genetic Test Cost
The SFXN4 Gene Combined Oxidative Phosphorylation Deficiency Type 18 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE. This test focuses on identifying mutations in the SFXN4 gene, which are linked to Combined Oxidative Phosphorylation Deficiency Type 18, a rare genetic disorder that affects mitochondrial function. This condition can lead to a wide range of clinical symptoms, including muscle weakness, neurological impairment, and systemic energy metabolism issues. The test employs advanced genetic sequencing techniques to analyze the SFXN4 gene, providing crucial information for the accurate diagnosis and potential management of the disorder. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed insights it provides into the patient's genetic makeup. By identifying specific genetic mutations, healthcare providers can better understand the condition's progression and explore targeted treatment options, offering hope for affected individuals and their families. DNA Labs UAE, known for its state-of-the-art facilities and expert team, ensures high-quality testing and reliable results for patients undergoing this genetic assessment.
LYRM4 Gene Combined oxidative phosphorylation deficiency type 19 Genetic Test Cost
The LYRM4 gene plays a crucial role in the proper functioning of the mitochondrial respiratory chain, which is essential for energy production within cells. Mutations in this gene can lead to Combined Oxidative Phosphorylation Deficiency Type 19 (COXPD19), a rare genetic disorder that affects multiple body systems, leading to a wide range of health issues including developmental delay, muscle weakness, and metabolic abnormalities. To diagnose this condition, a genetic test specifically targeting the LYRM4 gene is available. This test can confirm the presence of mutations in the LYRM4 gene, providing crucial information for diagnosis, treatment planning, and genetic counseling. The test involves analyzing the patient's DNA, typically extracted from a blood sample, to identify any genetic alterations in the LYRM4 gene that are known to cause COXPD19. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost for the LYRM4 gene test is 4400 AED. DNA Labs UAE is equipped with advanced genetic testing technologies and staffed by experts in the field, ensuring accurate and reliable results. This test is a valuable tool for families seeking answers to complex health issues related to COXPD19, enabling them to make informed decisions about their health care and management of the condition.
MRPS16 Gene Combined oxidative phosphorylation deficiency type 2 Genetic Test Cost
The MRPS16 gene plays a critical role in the mitochondrial ribosome, crucial for protein synthesis within mitochondria, which are the powerhouses of the cell. Mutations in the MRPS16 gene can lead to combined oxidative phosphorylation deficiency type 2 (COXPD2), a rare genetic disorder that affects multiple systems in the body. This condition is characterized by severe lactic acidosis, developmental delay, and failure to thrive, among other symptoms. To diagnose this condition, a genetic test targeting the MRPS16 gene can be conducted. This test involves analyzing the DNA to identify mutations in the MRPS16 gene that are known to cause COXPD2. Early diagnosis through genetic testing is crucial for the management of the disease, as it can guide treatment options and help in understanding the prognosis. In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test. The cost of the MRPS16 gene test is 4400 AED. Conducted in a state-of-the-art facility, DNA Labs UAE ensures accurate and reliable testing, adhering to the highest standards of genetic analysis. This test is essential for families with a history of mitochondrial disorders or for individuals showing symptoms suggestive of COXPD2, providing them with crucial information for managing the condition.
VARS2 Gene Combined oxidative phosphorylation deficiency type 20 Genetic Test Cost
The VARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 20 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the VARS2 gene. These mutations are associated with Combined Oxidative Phosphorylation Deficiency Type 20 (COXPD20), a rare genetic disorder that affects the body's energy production. This condition is part of a group of disorders that impair the oxidative phosphorylation process, which is crucial for generating the majority of the cell's supply of adenosine triphosphate (ATP), used as a source of chemical energy. The VARS2 gene plays a significant role in mitochondrial function and energy production, making its mutations particularly impactful on cellular energy levels. Individuals with COXPD20 may experience a wide range of symptoms, including developmental delay, muscle weakness, and metabolic abnormalities, among others. Early and accurate diagnosis through genetic testing is essential for the management of the condition, allowing for tailored treatment plans and interventions. The test is priced at 4400 AED and is conducted at DNA Labs UAE, a facility known for its advanced genetic testing services. By analyzing a sample of the patient's DNA, the test can pinpoint specific mutations in the VARS2 gene, providing crucial information for diagnosis, prognosis, and treatment planning. DNA Labs UAE employs state-of-the-art technology and methodologies to ensure high accuracy and reliability of the test results, making it a valuable resource for individuals suspected of having COXPD20 or for families with a history of the condition.
TARS2 Gene Combined oxidative phosphorylation deficiency type 21 Genetic Test Cost
The TARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 21 Genetic Test is a sophisticated diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the TARS2 gene. These mutations are implicated in Combined Oxidative Phosphorylation Deficiency 21 (COXPD21), a rare genetic disorder that affects mitochondrial function, leading to a wide range of clinical symptoms including developmental delay, muscle weakness, and metabolic abnormalities. This test is crucial for individuals suspected of having COXPD21, as it provides definitive genetic evidence of the condition, enabling accurate diagnosis and the possibility of tailored treatment plans. Conducted through advanced genomic techniques, the test examines the TARS2 gene for specific mutations known to cause the disorder. The cost of the TARS2 Gene Combined Oxidative Phosphorylation Deficiency Type 21 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis and the provision of a detailed report, which is instrumental in understanding the genetic basis of the condition and guiding further medical management. By choosing DNA Labs UAE for this test, patients and healthcare providers can expect high-quality service, precise results, and the expertise needed to interpret genetic information in the context of this complex disorder.
ATP5F1A Gene Combined oxidative phosphorylation deficiency type 22 Genetic Test Cost
The ATP5F1A gene plays a critical role in the process of oxidative phosphorylation, which is a vital part of cellular energy production in the mitochondria. Mutations in this gene can lead to Combined Oxidative Phosphorylation Deficiency Type 22 (COXPD22), a rare genetic disorder that affects multiple body systems and can result in a wide range of symptoms, including muscle weakness, heart problems, and developmental delays. To diagnose COXPD22, a genetic test targeting the ATP5F1A gene can be conducted. This test involves analyzing the DNA to identify mutations in the ATP5F1A gene that are responsible for the condition. It provides crucial information for the diagnosis, management, and treatment planning for individuals suspected of having this condition. In the UAE, DNA Labs offers this specific genetic test. The cost of the test is 4400 AED. Conducting the test at DNA Labs UAE ensures that individuals receive accurate and reliable results, utilizing state-of-the-art genetic testing technologies. The test is a significant step towards personalized medicine, enabling tailored treatment plans that address the specific needs of individuals affected by COXPD22.
GTPBP3 Gene Combined oxidative phosphorylation deficiency type 23 Genetic Test Cost
The GTPBP3 gene plays a crucial role in mitochondrial protein synthesis, which is essential for the proper function of the oxidative phosphorylation system. Mutations in the GTPBP3 gene can lead to Combined Oxidative Phosphorylation Deficiency 23 (COXPD23), a rare genetic disorder characterized by a wide range of clinical manifestations, including muscle weakness, heart problems, and developmental delays. To diagnose this condition, a genetic test focusing on the GTPBP3 gene can be conducted. DNA Labs UAE offers this specific test, providing a crucial tool for the accurate diagnosis of COXPD23. The test involves analyzing the patient's DNA to identify mutations in the GTPBP3 gene that are associated with the disorder. The cost of the GTPBP3 gene test at DNA Labs UAE is 4400 AED. This price includes the collection of a DNA sample, usually through a blood draw or cheek swab, and its subsequent analysis in the lab. The results from this test can help guide treatment decisions and allow for genetic counseling for affected families, offering insight into the risk of COXPD23 in future pregnancies. It's an essential step for families seeking answers to complex health issues related to oxidative phosphorylation deficiencies.
