The NDUFAF1 Gene Leigh Syndrome Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the NDUFAF1 gene, which are associated with Leigh syndrome, a severe neurological disorder. This genetic test is critical for early detection and management of the syndrome, offering insights into the genetic makeup of the individual and enabling healthcare professionals to devise tailored treatment plans. Conducted at DNA Labs UAE, a leading facility in genetic testing, the test ensures accuracy and reliability in results. The cost of the test is 4400 AED, reflecting the advanced technology and expertise involved in diagnosing this complex condition. Through this test, families affected by Leigh syndrome can gain a better understanding of their genetic predisposition and explore potential therapeutic interventions.
The NDUFAF2 Gene Leigh Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the NDUFAF2 gene, which are linked to Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically emerges in the first year of life, characterized by progressive loss of mental and movement abilities. The condition can result from genetic mutations affecting the mitochondrial function, with the NDUFAF2 gene playing a crucial role in mitochondrial complex I assembly.
This genetic test is vital for early detection and management of Leigh syndrome, allowing for a better understanding of the condition and aiding in the development of a tailored treatment plan for affected individuals. By analyzing the patient's DNA, the test can confirm the presence of mutations in the NDUFAF2 gene, providing essential information for families and healthcare providers.
The cost of the NDUFAF2 Gene Leigh Syndrome Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the sophisticated genetic analysis required to pinpoint the specific mutations associated with the disorder. Given the complexity and the specialized nature of this test, it represents a critical step forward in the care and management of patients potentially suffering from Leigh syndrome, offering hope and direction for affected families.
The NDUFS3 gene Leigh syndrome genetic test is a specialized diagnostic examination designed to identify mutations in the NDUFS3 gene, which are associated with Leigh syndrome. Leigh syndrome is a severe neurological disorder that typically emerges in infancy, characterized by progressive loss of mental and movement abilities. Mutations in the NDUFS3 gene disrupt the normal function of mitochondria, leading to the symptoms of the disorder.
This genetic test involves analyzing the patient's DNA to detect mutations in the NDUFS3 gene that are known to cause Leigh syndrome. The process aids in the accurate diagnosis of the syndrome, enabling healthcare providers to tailor management and treatment plans according to the specific needs of the patient.
The test is available at DNA Labs UAE, a leading facility in genetic diagnostics, providing advanced genetic testing services. The cost of the NDUFS3 gene Leigh syndrome genetic test is 4400 AED. Conducting this test at DNA Labs UAE ensures that patients receive reliable results, thanks to the lab's commitment to using cutting-edge technology and adhering to high standards of genetic analysis.
Leigh syndrome, a severe neurological disorder, is often linked to genetic mutations, one of which involves the NDUFS4 gene. This gene plays a crucial role in cellular energy production, and its mutations can lead to the development of Leigh syndrome, characterized by progressive loss of mental and movement abilities. To identify the presence of mutations in the NDUFS4 gene, DNA Labs UAE offers a specialized genetic test. This test is a critical tool for diagnosing Leigh syndrome, enabling early intervention and management of the condition. The cost of the NDUFS4 Gene Leigh Syndrome Genetic Test at DNA Labs UAE is 4400 AED. By providing accurate genetic diagnosis, this test is a cornerstone in the management and understanding of Leigh syndrome, offering hope and direction for affected families.
The NDUFS7 Gene Leigh Syndrome Genetic Test is a specialized diagnostic examination available at DNA Labs UAE, designed to detect mutations in the NDUFS7 gene that are associated with Leigh syndrome, a severe neurological disorder. Leigh syndrome, also known as subacute necrotizing encephalomyelopathy, is a progressive disease characterized by the degeneration of the central nervous system. It is genetically heterogeneous, meaning it can be caused by mutations in various genes, including NDUFS7, which plays a crucial role in mitochondrial function and energy production.
The test is particularly important for individuals with a family history of Leigh syndrome or those showing symptoms of the disease, such as developmental delay, muscle weakness, and difficulties with movement and breathing. Early and accurate diagnosis through the NDUFS7 Gene Leigh Syndrome Genetic Test can lead to better management of symptoms and improved quality of life for affected individuals.
Conducted at DNA Labs UAE, a leading facility in genetic testing, the test offers a reliable analysis of the NDUFS7 gene. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations associated with the condition. This genetic test represents a critical step towards personalized medicine, enabling tailored treatment plans based on an individual's genetic makeup, and providing families with essential information about the inheritance pattern and risks of Leigh syndrome.
The OFD1 Gene Joubert Syndrome Type 10 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at detecting mutations in the OFD1 gene, which are associated with Joubert Syndrome Type 10. This condition is a rare genetic disorder characterized by the underdevelopment of the cerebellum and brain stem, leading to a range of neurological symptoms, including coordination and balance issues, abnormal eye movements, and developmental delays. The test plays a crucial role in the early diagnosis and management of the syndrome, allowing for targeted interventions and support to improve the quality of life for affected individuals. Priced at 4400 AED, this test is a valuable resource for families seeking answers to complex genetic questions, providing them with critical information on their genetic health and predispositions.
The TCTN1 gene Joubert Syndrome Type 13 genetic test is a specialized diagnostic tool designed to identify mutations in the TCTN1 gene, which are associated with Joubert Syndrome Type 13. This rare genetic disorder is characterized by a variety of symptoms, including developmental delays, coordination problems, abnormal eye movements, and the distinctive "molar tooth sign" visible on brain imaging. Early and accurate diagnosis through genetic testing can aid in the management of symptoms and the provision of appropriate care and interventions.
The test is conducted at DNA Labs UAE, a leading facility in genetic diagnostics, ensuring high accuracy and reliability of results. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expertise required to identify the specific genetic alterations linked to this condition. This test is crucial for families seeking to understand their genetic health, enabling informed decisions regarding treatment and support for affected individuals.
The CEP41 gene is associated with Joubert Syndrome Type 15 (JBTS15), a rare genetic disorder characterized by the malformation of the cerebellum and brain stem, leading to a range of neurological symptoms, including coordination and balance issues, abnormal eye movements, and developmental delays. Genetic testing for mutations in the CEP41 gene is crucial for the diagnosis of JBTS15, enabling healthcare providers to offer accurate prognoses, personalized treatment plans, and genetic counseling for affected families.
DNA Labs UAE offers a specialized genetic test targeting the CEP41 gene to diagnose Joubert Syndrome Type 15. The test involves analyzing the patient's DNA to identify mutations in the CEP41 gene that are known to cause the condition. This test is vital for confirming the diagnosis of JBTS15, particularly in individuals showing the syndrome's characteristic symptoms or with a family history of the condition.
The cost of the CEP41 gene test for Joubert Syndrome Type 15 at DNA Labs UAE is 4400 AED. This price includes the full genetic analysis and a comprehensive report that can be used by healthcare professionals to guide treatment and management decisions for the patient. It is important for individuals considering this test to consult with a genetic counselor or healthcare provider to understand the implications of the results and the next steps in care and management.
The TMEM138 Gene Joubert Syndrome Type 16 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the TMEM138 gene, which are linked to Joubert Syndrome Type 16. This rare genetic disorder is part of a group of conditions known as ciliopathies, characterized by abnormalities in the structure and function of cilia, leading to a range of developmental issues, particularly affecting the cerebellum, an area of the brain that controls balance and coordination.
Joubert Syndrome manifests through a variety of symptoms, including developmental delays, coordination problems, abnormal breathing patterns, and distinctive facial features. The TMEM138 gene plays a critical role in the development and function of cilia; thus, mutations in this gene can disrupt normal cellular processes, leading to the symptoms observed in affected individuals.
The genetic test provided by DNA Labs UAE involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in their state-of-the-art laboratory. The test specifically looks for mutations in the TMEM138 gene that are known to cause Joubert Syndrome Type 16. This precise approach allows for an accurate diagnosis, which is crucial for the management and treatment of the condition.
The cost of the TMEM138 Gene Joubert Syndrome Type 16 Genetic Test at DNA Labs UAE is 4400 AED. While the test comes at a significant cost, the information it provides can be invaluable for affected families, offering insights into the condition and guiding decisions regarding care and treatment. Early diagnosis through genetic testing can also enable timely intervention, potentially improving outcomes for individuals with Joubert Syndrome Type 16.
The CPLANE1 Gene Joubert Syndrome Type 17 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the CPLANE1 gene, which are associated with Joubert Syndrome Type 17. Joubert Syndrome is a rare genetic disorder characterized by the underdevelopment of the cerebellum and brain stem, leading to a range of developmental delays and physical disabilities. This particular test is crucial for early diagnosis and management of the condition, allowing for tailored therapeutic strategies and support.
Priced at 4400 AED, the test involves collecting a DNA sample from the patient, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for genetic abnormalities in the CPLANE1 gene. The process is conducted with high precision and confidentiality, ensuring reliable results for affected families. Given the complexity of Joubert Syndrome and its impact on individuals’ quality of life, this genetic test is a valuable tool for genetic counseling and planning future medical care.
