The MAGT1 gene, associated with X-linked mental retardation type 95 (MRX95), plays a critical role in cognitive development and function. Mutations in the MAGT1 gene can lead to various neurological and developmental disorders, prominently featuring intellectual disabilities. Recognizing the importance of early and accurate diagnosis, DNA Labs UAE offers a specialized genetic test aimed at detecting mutations within the MAGT1 gene.
This genetic test is a powerful tool for families and healthcare professionals, providing crucial insights into the genetic underpinnings of intellectual disabilities linked to MRX95. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic alterations in the MAGT1 gene.
Priced at 4400 AED, the test is an investment in understanding and managing the implications of MRX95, offering a pathway towards personalized care plans and interventions. By pinpointing the genetic cause, families can access targeted support and resources, potentially improving outcomes and quality of life for affected individuals. DNA Labs UAE stands at the forefront of genetic diagnostics, providing this essential service with accuracy and confidentiality.
The SYP Gene Mental Retardation X-Linked Type 96 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, aimed at identifying mutations in the SYP gene, which are associated with X-linked mental retardation type 96. This condition is a rare genetic disorder that affects cognitive development and can lead to various degrees of intellectual disability, primarily in males due to its X-linked inheritance pattern. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any abnormalities in the SYP gene that could indicate the presence of the disorder.
With a test cost of 4400 AED, the procedure is a critical resource for families seeking answers about intellectual disabilities and related developmental issues. It not only aids in the diagnosis but also helps in understanding the condition's severity and potential management strategies. Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities and stringent quality controls, this test represents a crucial step towards personalized medicine and provides essential information for affected individuals and their families regarding prognosis and potential genetic counseling needs.
The ZNF711 Gene Mental Retardation X-Linked Type 97 Genetic Test is a specialized diagnostic tool designed to identify mutations in the ZNF711 gene, which is associated with X-linked mental retardation type 97. This condition is characterized by intellectual disabilities that are transmitted through the X chromosome, primarily affecting males. The ZNF711 gene plays a crucial role in brain development and function, and mutations in this gene can lead to a spectrum of cognitive impairments.
The test is conducted at DNA Labs UAE, a state-of-the-art facility equipped with advanced genetic testing technology. By analyzing a sample of the patient's DNA, the test can detect alterations in the ZNF711 gene that are indicative of X-linked mental retardation type 97. This information is vital for understanding the genetic basis of the condition, guiding treatment options, and providing genetic counseling for affected families.
The cost of the ZNF711 Gene Mental Retardation X-Linked Type 97 Genetic Test is 4400 AED. This investment covers the comprehensive analysis required to identify the genetic mutation responsible for the condition. Early and accurate diagnosis through this genetic test can significantly impact the management and support for individuals with this form of mental retardation, offering insights into potential therapeutic approaches and helping families make informed decisions about care and support.
The USP9X Gene Mental Retardation X-Linked Type 99 Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the USP9X gene, which have been associated with X-linked mental retardation type 99. This condition, primarily affecting males due to its X-linked inheritance pattern, is characterized by intellectual disabilities, developmental delays, and sometimes physical abnormalities. The genetic test involves analyzing the patient's DNA to detect any alterations in the USP9X gene that could lead to the condition. With a cost of 4400 AED, this test is crucial for families seeking to understand the genetic underpinnings of intellectual disabilities and for guiding future healthcare and support plans. DNA Labs UAE employs state-of-the-art genetic testing technologies to ensure accurate and reliable results for patients and their families.
The ATP6AP2 gene is associated with a rare X-linked form of mental retardation that often presents with epilepsy. Mutations in this gene can lead to a variety of neurological symptoms, including cognitive impairment and seizures. Understanding the genetic basis of these conditions is crucial for accurate diagnosis, management, and treatment.
The genetic test for the ATP6AP2 gene aims to identify mutations that might be responsible for mental retardation and epilepsy in affected individuals. This test is particularly useful for families with a history of these conditions, providing them with vital information that can guide clinical decisions and genetic counseling.
Performed at DNA Labs UAE, the test is available for a cost of 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology to ensure accurate and reliable testing results. The facility adheres to strict quality control measures, providing confidence in the test outcomes. This test represents a significant step forward in the personalized care of individuals with X-linked mental retardation and epilepsy, offering hope for better management and understanding of these complex conditions.
The AFF2 Gene Mental Retardation X-Linked Associated with Fragile Site FRAXE Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the AFF2 gene, which are linked to a form of X-linked mental retardation associated with the fragile site FRAXE. This condition is characterized by intellectual disabilities that can range from mild to severe and is caused by a genetic abnormality on the X chromosome. The test is particularly crucial for families with a history of intellectual disabilities, as it can provide definitive genetic evidence of the condition and help in managing and understanding the individual's needs.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the individual's DNA to detect the specific mutations in the AFF2 gene. The process is thorough and requires a sample of the individual's blood or saliva, which is then subjected to advanced genetic sequencing techniques to pinpoint the mutation.
The cost of the AFF2 Gene Mental Retardation X-Linked Associated with Fragile Site FRAXE Genetic Test is 4400 AED. While the price might seem high, the value of the information it provides for affected families is immeasurable. It not only aids in the diagnosis of the condition but also helps in understanding the genetic makeup, which is crucial for future family planning and management of the disorder. This test is a key step towards personalized care and support for individuals with this specific form of intellectual disability.
The EFHC2 gene, located on the X chromosome, has been associated with X-linked mental retardation. The gene's role in cognitive development is still being explored, but mutations in EFHC2 are believed to contribute to various neurological and developmental disorders. Recognizing the importance of early diagnosis and intervention, DNA Labs UAE offers a specialized genetic test focused on identifying mutations in the EFHC2 gene. This test is particularly relevant for families with a history of X-linked mental retardation, providing them with crucial information that can guide management and treatment options.
The test is conducted using a sample of the patient's DNA, typically extracted from a blood sample. Advanced molecular techniques are employed to meticulously analyze the EFHC2 gene for any abnormalities that might indicate a predisposition to mental retardation and other related conditions. This targeted approach allows for a high degree of specificity and accuracy in diagnosing conditions related to the EFHC2 gene.
Priced at 4400 AED, the EFHC2 related genetic test at DNA Labs UAE is an investment in understanding and potentially mitigating the impact of X-linked mental retardation in affected individuals and their families. The cost reflects the sophisticated technology and expertise required to conduct such specialized genetic testing. For families dealing with the challenges of X-linked mental retardation, this test offers a pathway to gaining valuable insights into their condition, enabling informed decisions about care and support.
The NEXMIF Gene Mental Retardation X-Linked Nonsyndromic Genetic Test is a specialized diagnostic tool used to identify mutations in the NEXMIF gene, which is linked to nonsyndromic mental retardation. This condition primarily affects males and is characterized by varying degrees of cognitive impairment without the presence of other physical or behavioral syndromes. The test is crucial for families seeking to understand the genetic basis of intellectual disabilities and for guiding potential therapeutic interventions or support services.
Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific mutations in the NEXMIF gene. The process is meticulous and leverages advanced genetic sequencing technologies to ensure accurate results.
The cost of the NEXMIF Gene Mental Retardation X-Linked Nonsyndromic Genetic Test is 4400 AED. While the price may seem high, the value of the insights gained for affected families cannot be overstated. It not only aids in the understanding of the condition but also assists in making informed decisions regarding management and support, potentially improving the quality of life for those affected.
The PHF8 Gene Mental Retardation X-Linked Siderius Type Genetic Test is a specialized diagnostic tool used to identify mutations in the PHF8 gene, which are linked to Siderius type X-linked mental retardation (XLMR). This condition is characterized by cognitive impairments, facial dysmorphisms, and, in some cases, cleft lip and palate. The test is critical for families seeking to understand genetic influences on developmental delays and intellectual challenges in affected individuals.
Performed at DNA Labs UAE, a leading facility in genetic diagnostics, this test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific genetic anomalies associated with the condition. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed reporting provided.
Identifying the genetic basis of XLMR through the PHF8 gene test allows for tailored support and interventions, enhancing the quality of life for individuals with the condition. Additionally, it provides essential information for family planning and the assessment of risk in future offspring. DNA Labs UAE ensures confidentiality and support throughout the testing process, offering a crucial resource for families navigating the complexities of genetic disorders.
The SMS Gene Mental Retardation X-Linked Snyder-Robinson Type Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the SMS gene, which are linked to Snyder-Robinson Syndrome (SRS). SRS is a rare form of X-linked intellectual disability that primarily affects males, presenting with features such as developmental delay, muscle weakness, skeletal abnormalities, and facial dysmorphisms. The test is crucial for families seeking to understand genetic predispositions and for clinicians in making accurate diagnoses to manage and support individuals with SRS effectively.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the individual's DNA to detect specific mutations in the SMS gene that are responsible for the condition. The process requires a sample of the individual's blood or saliva, which is then examined using advanced genetic sequencing technologies to identify any genetic abnormalities.
The cost of the SMS Gene Mental Retardation X-Linked Snyder-Robinson Type Genetic Test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the SMS gene. While the cost may seem significant, the test provides invaluable insights for affected individuals and their families, offering a clearer understanding of the condition and guiding potential treatment and management strategies.
