The TUBB gene plays a crucial role in the proper development and functioning of the nervous system. Mutations in this gene can lead to a range of neurodevelopmental disorders, which may affect an individual's cognitive, motor, and social abilities. Recognizing the importance of early diagnosis and intervention, DNA Labs UAE offers a specialized genetic test specifically designed to identify mutations in the TUBB gene. This test is a crucial tool for individuals who exhibit symptoms of neurodevelopmental disorders, as it can provide definitive answers regarding the presence of TUBB-related conditions.
The testing process involves a simple sample collection, after which the sample is analyzed using advanced genetic sequencing techniques to identify any mutations in the TUBB gene. This detailed analysis can help in understanding the specific nature of the disorder, thereby aiding in the formulation of a more personalized and effective treatment plan.
The cost of the TUBB gene neurodevelopmental disorder-related genetic test at DNA Labs UAE is 4400 AED. While the price may seem significant, the value of the insights gained from this test cannot be understated. It not only facilitates early diagnosis but also opens the door to targeted interventions that can significantly improve the quality of life for individuals affected by TUBB gene-related neurodevelopmental disorders.
The ZNF311 gene plays a crucial role in neurodevelopmental processes, and mutations in this gene have been associated with various neurodevelopmental disorders. These disorders can manifest as a range of cognitive, motor, and social impairments, underscoring the importance of accurate diagnosis and intervention. The ZNF311-Related Genetic Test is a specialized diagnostic tool designed to detect mutations in the ZNF311 gene, providing vital information for the diagnosis and management of associated neurodevelopmental conditions.
Administered at DNA Labs UAE, this test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed using advanced genetic sequencing technologies. This allows for the precise identification of any mutations in the ZNF311 gene that may be contributing to neurodevelopmental disorders.
The cost of the ZNF311-Related Genetic Test is 4400 AED. While the price may seem significant, the value of the information it provides cannot be overstated for families seeking answers to complex neurodevelopmental challenges. The results of this test can guide clinical decisions, inform therapeutic interventions, and offer families insights into the genetic underpinnings of their loved one's condition. It is a critical step towards personalized medicine in the realm of neurodevelopmental disorders, offering hope and direction for affected individuals and their families.
The "KIF2A Gene Neurodevelopmental Malformation and Microcephaly Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the KIF2A gene, which are associated with neurodevelopmental disorders and microcephaly. Microcephaly is a medical condition where a child's head is significantly smaller than expected, often due to abnormal brain development. Mutations in the KIF2A gene can lead to a spectrum of neurodevelopmental malformations, impacting a child's growth, brain structure, and cognitive development.
This genetic test is crucial for early detection and management of conditions linked to the KIF2A gene. By analyzing a patient's DNA, the test can pinpoint specific mutations in the KIF2A gene, providing essential information for accurate diagnosis, prognosis, and tailoring appropriate therapeutic strategies. This test is particularly valuable for families with a history of neurodevelopmental disorders, offering them insights into potential genetic risks for their children.
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 set at 4400 AED, reflecting the sophisticated technology and expertise involved in conducting such specialized genetic analyses. By opting for this test, families and healthcare providers can make informed decisions regarding the management and care of individuals with neurodevelopmental malformations and microcephaly, potentially improving quality of life and outcomes for affected individuals.
The KIF5C Gene Neurodevelopmental Malformation and Microcephaly Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the KIF5C gene, which are known to be associated with neurodevelopmental disorders, including malformations and microcephaly. Microcephaly is a condition where a baby's head is significantly smaller than expected, often due to abnormal brain development. The KIF5C gene plays a crucial role in neuronal migration and the proper formation of neural networks, which are essential for normal brain development.
This genetic test is crucial for early detection and understanding of specific neurodevelopmental conditions, allowing for timely intervention and support for affected individuals and their families. By analyzing a patient's DNA, the test can pinpoint mutations in the KIF5C gene that may lead to these developmental issues, providing a clear genetic diagnosis. This information is invaluable for guiding treatment options, managing symptoms, and improving the quality of life for those affected.
The test is priced at 4400 AED, reflecting the specialized nature of the genetic analysis and the profound impact that the results can have on patient care and family planning. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test ensures accuracy, confidentiality, and support throughout the testing process, making it a vital resource for families dealing with or at risk of neurodevelopmental disorders linked to the KIF5C gene.
The TUBG1 gene plays a crucial role in the normal development of the brain and nervous system. Mutations in this gene have been linked to neurodevelopmental malformations and microcephaly, a condition characterized by a smaller head size indicative of abnormal brain development. To diagnose and understand the genetic basis of these conditions, a specific genetic test targeting the TUBG1 gene is available.
This test, conducted at DNA Labs UAE, is designed to identify mutations in the TUBG1 gene that may lead to neurodevelopmental issues and microcephaly. By analyzing a sample of the patient's DNA, the test can provide crucial information for diagnosis, management, and treatment planning for affected individuals and their families. The cost of the TUBG1 gene neurodevelopmental malformation and microcephaly genetic test is 4400 AED. This test is a valuable tool for healthcare providers and patients in understanding and addressing the genetic components of these complex conditions.
The DES Gene Neurogenic Scapuloperoneal Syndrome Kaeser Type Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to identify mutations in the DES gene, which are associated with Neurogenic Scapuloperoneal Syndrome Kaeser Type (NSPKT). This condition is a rare genetic disorder characterized by muscle weakness and atrophy, primarily affecting the shoulder girdle and lower legs. It can also involve cardiac and respiratory muscles in some cases, making early detection and management crucial.
The test involves analyzing the patient's DNA to look for specific genetic alterations in the DES gene that are known to cause NSPKT. This is vital for confirming the diagnosis, understanding the disease's progression, and guiding treatment strategies. It also provides essential information for family planning and genetic counseling for affected families.
The cost of the DES Gene Neurogenic Scapuloperoneal Syndrome Kaeser Type Genetic Test at DNA Labs UAE is 4400 AED. The testing process is conducted with the highest standards of accuracy and confidentiality, ensuring patients receive comprehensive support throughout the diagnostic journey. Given the complexity and rarity of the condition, having access to such a targeted genetic test represents a significant step forward in personalized medicine and the management of genetic disorders.
The "HINT1 Gene Neuromyotonia and Axonal Neuropathy Autosomal Recessive Genetic Test" is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the HINT1 gene. This gene is crucial because mutations within it are linked to the development of neuromyotonia and axonal neuropathy, conditions that affect the nervous system leading to muscle stiffness and weakness, among other symptoms. These disorders are inherited in an autosomal recessive pattern, meaning an individual must receive a mutated gene from both parents to be affected.
The test, which costs 4400 AED, is a vital tool for families with a history of these conditions, providing them with crucial information regarding their genetic status. Early detection through this genetic testing can facilitate timely intervention and management of the conditions, potentially improving the quality of life for those affected. DNA Labs UAE utilizes advanced genetic testing technologies to ensure accurate and reliable results, making it a trusted choice for individuals seeking clarity about their genetic health concerning the HINT1 gene.
The CTNNA2 gene is associated with critical functions in the nervous system, playing a vital role in the process of neuronal migration, a fundamental phase in brain development. Mutations in the CTNNA2 gene can lead to various neurological disorders, emphasizing the importance of genetic testing for early diagnosis and intervention.
The CTNNA2 Gene Neuronal Migration Disorder Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the CTNNA2 gene. This test is crucial for individuals who may have neurological conditions related to impaired neuronal migration, as it can provide definitive genetic evidence of such disorders. Early detection through this test can facilitate timely medical and therapeutic interventions, potentially improving patient outcomes.
The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the CTNNA2 gene. DNA Labs UAE, renowned for its commitment to precision and excellence in genetic diagnostics, ensures that this test is conducted under the highest standards of quality and reliability. By opting for this test, patients and their families can gain valuable insights into their genetic makeup, paving the way for personalized treatment strategies and better understanding of their conditions.
The "C19orf12 Gene Neurodegeneration with Brain Iron Accumulation Type 4 Genetic Test" is a specialized diagnostic examination conducted to identify mutations in the C19orf12 gene, which are associated with Neurodegeneration with Brain Iron Accumulation Type 4 (NBIA-4), also known as Mitochondrial Membrane Protein-Associated Neurodegeneration (MPAN). This condition is characterized by progressive neurodegeneration and the accumulation of iron in specific areas of the brain, leading to a range of neurological symptoms such as movement disorders, psychiatric symptoms, and cognitive decline.
The test is designed to provide crucial genetic information for the accurate diagnosis and management of individuals suspected to have or at risk of developing NBIA-4. By analyzing the C19orf12 gene, healthcare providers can confirm the diagnosis, understand the disease's progression, and potentially tailor treatment strategies to manage symptoms more effectively.
This genetic 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. DNA Labs UAE is equipped with state-of-the-art technology and staffed by professionals with expertise in genetic diagnostics, ensuring high-quality testing and reliable results for patients and their families.
The COASY Gene Neurodegeneration with Brain Iron Accumulation Type 6 (NBIA6) genetic test is a specialized diagnostic tool used to identify mutations in the COASY gene, which are linked to a rare form of neurodegeneration characterized by the accumulation of iron in the brain. This condition, known as NBIA6, can lead to a range of neurological symptoms, including movement disorders, psychiatric issues, and progressive deterioration of motor functions. The test is crucial for confirming a diagnosis, enabling early intervention, and facilitating appropriate management and treatment strategies for affected individuals.
Conducted at DNA Labs UAE, the test involves a detailed analysis of the patient's DNA to detect any abnormalities or mutations in the COASY gene that could indicate the presence of NBIA6. This state-of-the-art genetic testing provides families and healthcare professionals with essential information regarding the genetic basis of the condition, helping to guide treatment decisions and offering insights into potential genetic counseling needs for the family.
The cost of the COASY Gene Neurodegeneration with Brain Iron Accumulation Type 6 Genetic Test at DNA Labs UAE is 4400 AED. Given the specialized nature of the test and the expertise required to accurately interpret the results, this cost reflects the comprehensive analysis and personalized care that patients receive. For families facing the challenges of NBIA6, this test represents a critical step towards understanding and managing the condition more effectively.
