The MACF1 gene plays a critical role in the development and functioning of the nervous system. Mutations in this gene can lead to a spectrum of neurodevelopmental disorders, characterized by cognitive impairment, motor function difficulties, and sometimes autism spectrum disorders or other neurological symptoms. The MACF1-related genetic test is a specialized diagnostic tool designed to identify mutations in the MACF1 gene, providing crucial information for the diagnosis and management of associated neurodevelopmental conditions.
Conducted at DNA Labs UAE, this test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing the genetic material for specific mutations in the MACF1 gene. The outcome of this test can help healthcare providers develop a more tailored approach to the treatment and support of individuals affected by MACF1-related disorders.
The cost of the MACF1 genetic test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, from the initial collection of the DNA sample to the detailed analysis and reporting of results. Families and individuals considering this test should consult with a genetic counselor or healthcare provider to understand the potential implications of the results and to ensure that this testing is aligned with their healthcare goals.
The mTOR gene, central to the mTOR signaling pathway, plays a critical role in cell growth, proliferation, and neurodevelopment. Mutations in this gene can lead to a spectrum of neurodevelopmental disorders characterized by intellectual disability, autism, epilepsy, and other neurological issues. Given the significant impact these mutations can have on an individual's quality of life, early and accurate diagnosis is crucial.
DNA Labs UAE offers a specialized genetic test targeting the mTOR gene to identify mutations that may contribute to neurodevelopmental disorders. This test is a vital tool for individuals displaying symptoms associated with mTOR-related conditions, enabling healthcare providers to make informed decisions regarding treatment and management strategies.
The cost of the mTOR-related genetic test at DNA Labs UAE is 4400 AED. This investment includes a comprehensive analysis of the mTOR gene, aiming to provide patients and their families with crucial information that can guide therapeutic interventions and support. By opting for this test, families gain access to personalized medicine, tailoring interventions to the unique genetic makeup of the individual, potentially improving outcomes and quality of life.
The NGEF Gene Neurodevelopmental Disorder is a condition linked to mutations in the NGEF gene, which plays a crucial role in the development and functioning of the nervous system. These mutations can lead to various neurodevelopmental issues, impacting an individual's cognitive, social, and motor skills from a very young age. Given the complexity and variability of symptoms associated with this disorder, accurate diagnosis is crucial for effective management and treatment.
To aid in the diagnosis of this condition, DNA Labs UAE offers a specialized genetic test specifically designed to identify mutations in the NGEF gene. This test is a critical tool for healthcare professionals in confirming the presence of the disorder, allowing for early intervention strategies that can significantly improve the quality of life for affected individuals.
The cost of the NGEF Related Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the advanced technology and expertise required to accurately analyze and interpret the genetic data. Families and individuals considering this test should consult with healthcare professionals to understand its benefits and implications fully.
By opting for this genetic test, patients and their families can gain valuable insights into their condition, enabling personalized treatment plans that cater to the specific needs of the individual. DNA Labs UAE, with its commitment to providing high-quality genetic testing services, plays a pivotal role in advancing the understanding and management of neurodevelopmental disorders.
The PIGQ gene plays a crucial role in the biosynthesis of GPI anchors, which are critical for attaching various proteins to the cell surface, thereby influencing numerous cellular processes, including signal transduction and cell-to-cell interaction. Mutations in the PIGQ gene can lead to a spectrum of neurodevelopmental disorders, characterized by symptoms ranging from intellectual disability, seizures, to issues with motor skills and speech. These disorders fall under the broader category of GPI anchor biosynthesis defects.
To diagnose conditions associated with PIGQ mutations, DNA Labs UAE offers a specialized genetic test. This test aims to identify mutations in the PIGQ gene, providing essential information for accurate diagnosis and potential management strategies for affected individuals. The cost of the PIGQ related genetic test is 4400 AED. Conducted in a state-of-the-art facility, the test involves analyzing the patient's DNA sample to detect any genetic alterations in the PIGQ gene, thereby enabling healthcare providers to make informed decisions regarding treatment and support for patients with neurodevelopmental disorders linked to PIGQ mutations.
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 "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.
