The "KLF8 Gene Mental Retardation Non-Syndromic Genetic Test" is a specialized diagnostic tool designed to identify mutations in the KLF8 gene, which have been associated with non-syndromic mental retardation. This condition is characterized by intellectual disabilities that occur without other significant physical or behavioral abnormalities. The KLF8 gene plays a crucial role in brain development and function, and mutations in this gene can lead to various neurodevelopmental disorders.
The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. It involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed using advanced genetic sequencing techniques to detect any abnormalities or mutations in the KLF8 gene.
The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations and provide reliable results. This test is particularly valuable for families seeking a deeper understanding of intellectual disabilities with an unknown cause, as it can provide crucial information for diagnosis, management, and treatment planning.
The "NXF5 Gene Mental Retardation Non-Syndromic Genetic Test" is a specialized diagnostic tool designed to identify mutations in the NXF5 gene, which have been linked to non-syndromic mental retardation. This condition is characterized by intellectual disabilities that occur without additional physical or neurological symptoms typically associated with syndromic forms of mental retardation. The test is conducted by extracting a DNA sample from the patient, which is then analyzed in a laboratory setting to detect any abnormalities or mutations in the NXF5 gene that could be responsible for the condition.
Conducted at DNA Labs UAE, a leading facility in genetic testing, this test is crucial for families seeking to understand the genetic basis of intellectual disabilities in their loved ones. It can provide essential information for making informed decisions about care, support, and potential therapies. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed reporting that accompanies this advanced genetic assessment. By identifying specific genetic mutations, the test not only aids in the diagnosis of non-syndromic mental retardation but also contributes to a broader understanding of the genetic factors involved in intellectual disabilities.
The ZCCHC12 gene is associated with non-syndromic mental retardation, a condition characterized by intellectual disabilities that do not coincide with other physical or neurological symptoms. Genetic testing for mutations in the ZCCHC12 gene can help in diagnosing this specific form of mental retardation, allowing for better-informed decisions regarding management and care. DNA Labs UAE offers a specialized genetic test to identify mutations in the ZCCHC12 gene. The cost of this test is 4400 AED. By undergoing this test, individuals can gain valuable insights into their genetic makeup, potentially leading to early intervention and support strategies that can improve quality of life.
The "WDR81 Gene Mental Retardation with Cerebellar Ataxia and Dysequilibrium Syndrome Type 2 Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the WDR81 gene. These mutations are linked to a rare genetic disorder characterized by intellectual disability, impaired coordination (cerebellar ataxia), and balance issues (dysequilibrium syndrome type 2). The test, priced at 4400 AED, is crucial for accurate diagnosis, enabling targeted management and therapy plans for affected individuals. Through advanced genetic analysis, DNA Labs UAE offers families and healthcare professionals vital information for understanding and addressing the complex needs associated with this condition.
The ATRX Gene Mental Retardation with Hypotonic Facies Syndrome X-Linked Genetic Test is a specialized diagnostic procedure designed to identify mutations in the ATRX gene, which are associated with a rare genetic condition. This condition, often referred to as ATR-X syndrome, is characterized by intellectual disability, facial dysmorphism, and other physical abnormalities. The test plays a crucial role in the early diagnosis and management of the syndrome, enabling healthcare professionals to provide targeted interventions and support for affected individuals.
Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities, the test involves collecting a DNA sample from the patient, usually through a blood draw or cheek swab. The sample is then analyzed for specific mutations in the ATRX gene that are known to cause the syndrome.
The cost of the ATRX Gene Mental Retardation with Hypotonic Facies Syndrome X-Linked Genetic Test is set at 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify the genetic mutations associated with the condition. Patients considering this test are advised to consult with their healthcare provider to understand its benefits and implications fully.
The FOXP1 gene test is a specialized genetic analysis designed to identify mutations in the FOXP1 gene, which is known to be associated with mental retardation, language impairment, and autistic features. This test is particularly relevant for individuals showing symptoms of these conditions, as it can provide a definitive diagnosis and help guide treatment and management strategies.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or a cheek swab, and then analyzing the genetic material for specific mutations in the FOXP1 gene. These mutations can disrupt normal brain development and function, leading to the observed symptoms.
The cost of the FOXP1 gene test at DNA Labs UAE is 4400 AED. While the price might seem significant, the value of the insights gained from this test can be immeasurable for affected individuals and their families. It not only aids in understanding the condition better but also opens up avenues for targeted interventions and supports that can significantly improve the quality of life for those diagnosed with disorders linked to the FOXP1 gene.
Given the complexity of the disorders associated with FOXP1 mutations, this test is a crucial tool in the arsenal of healthcare providers, enabling them to offer personalized care plans based on genetic information.
The SMARCA1 gene plays a crucial role in regulating gene expression and is involved in chromatin remodeling. Mutations in the SMARCA1 gene have been associated with X-linked mental retardation and other developmental disorders. The genetic test for SMARCA1-related conditions is designed to identify mutations in the SMARCA1 gene that may lead to intellectual disabilities and other symptoms associated with the disorder.
At DNA Labs UAE, a specialized genetic test is offered to diagnose conditions related to mutations in the SMARCA1 gene. This test is particularly important for families with a history of X-linked mental retardation or for individuals showing symptoms related to SMARCA1 mutations. Early diagnosis through genetic testing can aid in understanding the condition better, allowing for appropriate management and support.
The cost of the SMARCA1 Gene Mental Retardation X-linked SMARCA1 Related Genetic Test at DNA Labs UAE is 4400 AED. This comprehensive test is conducted by experienced professionals using advanced genetic testing technologies to ensure accuracy and reliability of the results. By opting for this test, individuals can gain valuable insights into their genetic makeup, paving the way for personalized medical care and interventions tailored to their specific needs.
The KDM5C Gene Mental Retardation X-linked Syndromic Claes-Jensen Type Genetic Test is a specialized diagnostic procedure designed to identify mutations in the KDM5C gene, which are linked to Claes-Jensen type mental retardation. This condition is an X-linked syndrome, meaning it primarily affects males and is passed down through the maternal line. Symptoms can include intellectual disability, developmental delays, and sometimes physical abnormalities.
This genetic test involves analyzing the patient's DNA, extracted from a blood sample, to look for specific mutations in the KDM5C gene that are known to cause the syndrome. The process is highly accurate and can provide crucial information for families regarding prognosis, management, and genetic counseling.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test ensures confidentiality, precision, and reliability. The cost of the test is set at 4400 AED, reflecting the sophisticated technology and expertise required to perform this intricate analysis. For families facing the challenges of X-linked mental retardation syndromes, this test represents a vital step towards understanding and managing the condition.
The MECP2 Gene Mental Retardation X-linked Syndromic Lubs Type Genetic Test is a specialized diagnostic tool designed to detect mutations in the MECP2 gene, which are associated with Lubs type X-linked mental retardation. This condition, part of a spectrum of MECP2-related disorders, is characterized by intellectual disability, developmental delays, and sometimes physical abnormalities. The test is crucial for early diagnosis and intervention, providing valuable information for managing the condition and counseling affected families.
Performed at DNA Labs UAE, a leading facility in genetic testing, this test employs advanced genetic sequencing techniques to analyze the MECP2 gene for any abnormalities that may indicate the presence of the disorder. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately identify mutations in the MECP2 gene. By opting for this test, individuals and families gain access to crucial genetic information that can guide clinical management and therapeutic strategies, ultimately enhancing the quality of life for those affected by Lubs type X-linked mental retardation.
The "SOBP Gene Mental Retardation, Anterior Maxillary Protrusion, and Strabismus Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the SOBP gene that are associated with a specific syndrome characterized by intellectual disability, forward protrusion of the upper jaw, and strabismus (crossed eyes). This genetic testing is crucial for early diagnosis and management of the condition, enabling healthcare providers to offer personalized treatment plans and supportive care for affected individuals. The test is conducted using advanced genomic technologies to analyze the patient's DNA, ensuring high accuracy and reliability. The cost of the test is 4400 AED, reflecting the comprehensive analysis and detailed insights it provides into the patient's genetic makeup, which can significantly impact their treatment and management plan.
