The CP Gene Cerebellar Ataxia Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the CP gene that are associated with the development of cerebellar ataxia. Cerebellar ataxia is a neurological disorder characterized by a lack of muscle coordination, which can affect speech, eye movements, the ability to swallow, walking, and other voluntary movements. This condition is often inherited and can be caused by mutations in various genes, including the CP gene.
The test is conducted through a comprehensive analysis of the patient's DNA, extracted from a blood sample, to detect specific genetic alterations in the CP gene that are known to contribute to the condition. The results from this test can provide crucial information for the diagnosis, management, and understanding of the individual's condition. It can also offer insights into the risk of passing the condition on to future generations, aiding in family planning decisions.
Priced at 4400 AED, the CP Gene Cerebellar Ataxia Genetic Test at DNA Labs UAE represents a significant investment in personal health and genetic understanding. It is a valuable resource for individuals showing symptoms of cerebellar ataxia or those with a family history of the disorder, offering them a clearer picture of their genetic health and enabling them to take informed steps towards managing their condition.
The "CA8 Gene Cerebellar Ataxia and Mental Retardation with or without Quadrupedal Locomotion Type 3 Genetic Test" is a specialized diagnostic tool offered by DNA Labs UAE, aimed at identifying mutations in the CA8 gene. These mutations are associated with a rare neurological disorder that can manifest as cerebellar ataxia, mental retardation, and in some cases, an unusual pattern of movement that may include quadrupedal locomotion. Cerebellar ataxia refers to a lack of muscle control or coordination of voluntary movements, which stems from problems in the cerebellum, the part of the brain that controls muscle coordination.
The test, priced at 4400 AED, involves analyzing the patient's DNA to detect abnormalities in the CA8 gene that could confirm the diagnosis of this condition. This genetic testing is crucial for families seeking to understand the genetic basis of the disorder, which can aid in managing the condition, anticipating its progression, and making informed decisions about care. Additionally, it can provide essential information for genetic counseling, especially for those planning to have children and concerned about passing on genetic conditions.
DNA Labs UAE, a leading facility in genetic testing, employs advanced technologies and methodologies to ensure accurate and reliable results. The test is conducted under the strictest standards of quality and confidentiality, ensuring that patients receive comprehensive support throughout the testing process.
The DNMT1 Gene Cerebellar Ataxia with Deafness and Narcolepsy Autosomal Recessive Genetic Test is a specialized diagnostic examination available at DNA Labs UAE, designed to identify mutations in the DNMT1 gene that are associated with a rare, autosomal recessive disorder. This condition is characterized by a combination of symptoms including cerebellar ataxia, which involves coordination and balance problems due to cerebellum damage; deafness; and narcolepsy, a chronic sleep disorder that causes overwhelming daytime drowsiness and sudden sleep attacks. The test is crucial for individuals who exhibit these symptoms or have a family history of the disorder, as it aids in the accurate diagnosis and management of the condition. The cost of the test is 4400 AED, reflecting the comprehensive analysis and expertise required to interpret the genetic data. Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers hope for affected individuals and their families by providing essential information for treatment planning and genetic counseling.
The WDR81 gene cerebellar ataxia with mental retardation and dysequilibrium syndrome type 2 genetic test is a specialized diagnostic tool available at DNA Labs UAE. This test is designed to identify mutations in the WDR81 gene, which are known to cause cerebellar ataxia with mental retardation and dysequilibrium syndrome type 2 (CAMRQ2). CAMRQ2 is a rare genetic disorder characterized by developmental delays, intellectual disability, and difficulties with coordination and balance due to cerebellar ataxia. The test is crucial for early diagnosis and management of the condition, offering insights that can guide therapeutic interventions and support. Priced at 4400 AED, the test involves analyzing the patient's DNA to detect abnormalities in the WDR81 gene, providing families and healthcare professionals with essential information for care planning and genetic counseling.
The "GBA2 Gene Cerebellar Ataxia with Spasticity Genetic Test" is a specialized diagnostic procedure aimed at individuals who exhibit symptoms of cerebellar ataxia combined with spasticity, suggesting a potential genetic underpinning. This test specifically targets the GBA2 gene, which has been linked to this neurological condition. Mutations in the GBA2 gene can disrupt normal brain function, leading to the symptoms observed in affected individuals. The test is designed to detect such mutations, providing crucial information for diagnosis, management, and treatment planning.
Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test is available for a cost of 4400 AED. DNA Labs UAE employs state-of-the-art technology and methodologies to ensure accurate and reliable results, making it a preferred choice for genetic testing in the region. By opting for this test, patients and their families can gain insights into the genetic basis of the condition, facilitating informed decisions regarding healthcare and potential therapeutic interventions.
The ATP8A2 gene plays a crucial role in neurological development and function. Mutations in this gene are associated with a rare genetic disorder known as Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome Type 4 (CAMRQ4). This condition is characterized by developmental delays, difficulty in coordination and balance (ataxia), and intellectual disabilities.
To diagnose this condition, genetic testing is available at DNA Labs UAE, a leading facility in genetic diagnostics. The test specifically looks for mutations in the ATP8A2 gene that are indicative of CAMRQ4. It involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the lab using advanced genetic sequencing techniques.
The cost of the ATP8A2 gene test at DNA Labs UAE is 4400 AED. This comprehensive testing not only aids in the diagnosis of CAMRQ4 but also helps in understanding the condition better, enabling tailored management and treatment plans for affected individuals. It is a crucial step for families seeking answers to developmental and neurological concerns in their loved ones.
The CAMTA1 gene cerebellar ataxia nonprogressive with mental retardation genetic test is a specialized diagnostic procedure aimed at identifying mutations in the CAMTA1 gene, which are associated with a rare genetic disorder. This condition is characterized by early-onset cerebellar ataxia, a disorder that affects coordination and balance, coupled with intellectual disabilities. Unlike other forms of ataxia, this particular type is nonprogressive, meaning symptoms do not worsen over time.
The test involves analyzing the patient's DNA to detect any abnormalities or mutations in the CAMTA1 gene that may be responsible for the symptoms. This genetic testing is crucial for accurate diagnosis, enabling healthcare providers to offer appropriate management strategies and support for affected individuals and their families.
Administered by DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures high accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the comprehensive analysis and expertise required to conduct this specialized genetic assessment. By opting for this test, patients and their families can gain valuable insights into their condition, paving the way for a better understanding and tailored care plans.
The SNX14 Gene Cerebellar Ataxia SNX14 Related Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the SNX14 gene, which are known to cause cerebellar ataxia. Cerebellar ataxia is a neurological disorder that affects coordination and balance, often leading to significant impairment in movement and motor functions. The SNX14 gene plays a crucial role in the proper functioning of the cerebellum, and mutations in this gene can disrupt its activity, leading to the symptoms associated with cerebellar ataxia.
This genetic test is particularly important for individuals who exhibit symptoms of cerebellar ataxia or have a family history of the condition, as it can provide a definitive diagnosis. Early detection through this genetic testing can facilitate timely intervention and management of the disorder, potentially improving the quality of life for those affected.
The test involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to identify any mutations in the SNX14 gene. The procedure is highly accurate and provides valuable genetic insights that can aid in the diagnosis and management of cerebellar ataxia.
At DNA Labs UAE, the cost of the SNX14 Gene Cerebellar Ataxia SNX14 Related Genetic Test is set at 4400 AED. While the cost may seem substantial, the test offers critical information for affected individuals and their families, guiding treatment decisions and offering a clearer understanding of the genetic underpinnings of their condition.
The NTNG1 gene, or Netrin G1, has been studied for its potential association with autism spectrum disorders (ASD). This gene plays a crucial role in the development of neural circuits, which are essential for proper brain function. Variations or mutations in the NTNG1 gene may contribute to the development of ASD by affecting neural connectivity and communication.
DNA Labs UAE offers a specialized genetic test targeting the NTNG1 gene to identify potential mutations or variations that could be linked to autism. This test is particularly useful for families with a history of ASD or for individuals who exhibit symptoms related to autism spectrum disorders. By analyzing the genetic makeup of the NTNG1 gene, the test aims to provide valuable insights into the genetic factors contributing to ASD, potentially guiding diagnosis, management, and intervention strategies.
The cost of the NTNG1-related genetic test at DNA Labs UAE is 4400 AED. This comprehensive test is performed in a state-of-the-art laboratory by experienced geneticists and technicians, ensuring high accuracy and reliability of the results. The test involves a simple sample collection process, after which the sample is analyzed to detect any significant alterations in the NTNG1 gene that could be associated with autism.
By opting for the NTNG1 gene autism-related genetic test, individuals and families can gain a deeper understanding of the genetic components of ASD, aiding in early detection and personalized approaches to treatment and support.
The OR13H1 gene is a specific genetic marker that has been identified as having a potential link to autism spectrum disorder (ASD). Research into the OR13H1 gene and its association with autism is part of a broader effort to understand the genetic factors that may contribute to the condition. Autism is a complex developmental disorder characterized by challenges with social interaction, communication, and repetitive behaviors. The exact cause of autism is unknown, but it is believed to be a combination of genetic and environmental factors.
DNA Labs UAE offers a specialized genetic test that focuses on the OR13H1 gene to assess its association with autism in individuals. This test is particularly valuable for families with a history of autism, as it can provide insights into the genetic predisposition of family members to the disorder. The test involves collecting a DNA sample from the individual, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any variations or mutations in the OR13H1 gene that might be linked to autism.
The cost of the OR13H1 related genetic test at DNA Labs UAE is 4400 AED. This price may cover the test procedure, analysis, and a comprehensive report that explains the findings. The report might also offer recommendations or guidance on the next steps, depending on the results. It's important for individuals considering this test to consult with a healthcare professional or a genetic counselor both before and after the test to fully understand the implications of the results and to receive appropriate support and advice.
