The PGAP1 gene plays a critical role in brain development and function. Mutations in this gene are associated with Mental Retardation, Autosomal Recessive Type 42 (MRT42), a condition characterized by intellectual disabilities and potentially other neurological or physical abnormalities. The genetic test for MRT42, specifically targeting the PGAP1 gene, is a crucial tool in diagnosing this condition.
Conducted at DNA Labs UAE, this test involves analyzing the patient's DNA to identify mutations in the PGAP1 gene that are indicative of MRT42. The process is aimed at individuals who exhibit symptoms of intellectual disability, their family members, or those with a known family history of the condition. By pinpointing the genetic cause, this test not only confirms the diagnosis but also helps in understanding the condition better, paving the way for personalized management and support strategies.
The cost of the PGAP1 Gene Mental Retardation Autosomal Recessive Type 42 Genetic Test at DNA Labs UAE is 4400 AED. While the price might seem steep, the value it provides in terms of accurate diagnosis, informed decision-making regarding care, and potential family planning considerations can be invaluable for affected individuals and their families.
The NDST1 Gene Mental Retardation Autosomal Recessive Type 46 Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the NDST1 gene, which have been linked to Autosomal Recessive Type 46 Mental Retardation. This condition is a rare genetic disorder characterized by intellectual disability and possibly other physical or neurological symptoms, with its inheritance pattern being autosomal recessive, meaning both parents must carry a copy of the mutated gene to pass the condition onto their offspring.
The test is performed at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities. The process involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the lab to detect any abnormalities in the NDST1 gene that could indicate the presence of the disorder.
The cost of the NDST1 Gene Mental Retardation Autosomal Recessive Type 46 Genetic Test is 4400 AED. This price reflects the comprehensive nature of the test, covering the expenses of the genetic analysis and the expertise required to accurately interpret the results. Given the complexity of genetic disorders and the specific expertise needed to diagnose them, the test provides valuable insights for affected families, offering a clear genetic diagnosis that can inform further medical and supportive care decisions.
The GPT2 Gene Mental Retardation Autosomal Recessive Type 49 Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the GPT2 gene, which have been linked to autosomal recessive intellectual disability type 49. This condition is characterized by developmental delays, learning disabilities, and possibly other neurological or physical abnormalities. The test is crucial for families seeking answers to genetic questions related to intellectual disabilities, allowing for better understanding, management, and planning for affected individuals' needs. The test is priced at 4400 AED, reflecting the sophisticated technology and expertise required to accurately analyze and interpret the genetic data. DNA Labs UAE, with its state-of-the-art facilities and experienced professionals, ensures a reliable and comprehensive assessment for those undergoing the test.
The NSUN2 gene is associated with a condition known as Mental Retardation, Autosomal Recessive Type 5 (MRD5). This condition is characterized by intellectual disabilities that can range from mild to severe, often accompanied by other neurological and physical abnormalities. The NSUN2 gene plays a crucial role in the proper development and function of the brain, and mutations in this gene can lead to the symptoms observed in MRD5.
To diagnose this condition accurately, genetic testing of the NSUN2 gene can be conducted. DNA Labs UAE offers a comprehensive genetic test specifically designed to identify mutations in the NSUN2 gene that are linked to Mental Retardation, Autosomal Recessive Type 5. The test is a critical tool for families seeking answers to developmental delays and intellectual challenges faced by their loved ones. It provides essential information for understanding the condition, potential interventions, and management strategies to improve the quality of life for those affected.
The cost of the NSUN2 gene test at DNA Labs UAE is 4400 AED. This investment covers the meticulous process of analyzing the genetic material to detect any abnormalities in the NSUN2 gene that could indicate the presence of MRD5. The test is conducted under the guidance of genetic specialists who ensure the accuracy and reliability of the results. Upon completion, a comprehensive report is provided, detailing the findings and their implications for the individual and their family. This report serves as a valuable resource for healthcare providers in devising a personalized care plan tailored to the specific needs of the patient.
The "PUS3 Gene Mental Retardation Autosomal Recessive Type 55 Genetic Test" is a specific diagnostic procedure conducted to identify mutations in the PUS3 gene, which are linked to Mental Retardation Autosomal Recessive Type 55 (MRAR55). This condition is characterized by intellectual disabilities, developmental delays, and possibly other physical or neurological symptoms, inherited in an autosomal recessive pattern. This means that an individual must inherit two copies of the mutated gene, one from each parent, to be affected by the condition.
The test is particularly valuable for families with a history of MRAR55, couples planning to have children who want to understand their risk of passing the condition to their offspring, and individuals showing symptoms related to intellectual disabilities who are seeking a precise diagnosis.
Conducted at DNA Labs UAE, a leading facility in genetic testing and diagnostics, the test involves collecting a DNA sample, typically through a blood draw or cheek swab, and analyzing it for specific mutations in the PUS3 gene. The cost of the test is 4400 AED, which reflects the comprehensive analysis and expertise required to accurately identify mutations in the PUS3 gene.
Choosing to undergo this genetic test can provide crucial information for affected individuals and their families, offering insights into the condition, informing treatment and management strategies, and aiding in the understanding of inheritance patterns and risks for future generations.
The TUSC3 gene mental retardation autosomal recessive type 7 genetic test is a specialized diagnostic procedure designed to identify mutations in the TUSC3 gene, which are linked to a specific form of intellectual disability known as autosomal recessive non-syndromic intellectual disability (ARNS-ID). This condition is characterized by developmental delays, learning disabilities, and sometimes physical anomalies, with the severity of symptoms varying among affected individuals.
This genetic test is crucial for families seeking answers about intellectual disabilities within their lineage, as it can provide a definitive diagnosis of the condition tied to the TUSC3 gene mutation. By detecting the presence of specific genetic alterations, healthcare providers can offer more targeted support and interventions, improving the quality of life for those affected.
The test is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the TUSC3 gene mental retardation autosomal recessive type 7 genetic test is 4400 AED. This investment covers the comprehensive analysis needed to detect mutations in the TUSC3 gene, providing families with crucial information for managing the condition and making informed decisions about care and support.
The RAB40AL gene, also known as the Mental Retardation X-Linked (MRX) gene, plays a crucial role in cognitive development. Mutations in this gene are associated with X-linked mental retardation, a condition that affects intellectual functioning and may be accompanied by physical or psychiatric comorbidities. The RAB40AL Gene Mental Retardation X-Linked Genetic Test is a specialized diagnostic tool designed to detect mutations in the RAB40AL gene. This test is particularly relevant for families with a history of X-linked mental retardation, offering them a chance to understand their genetic makeup and the risk of passing the condition to their offspring.
The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the RAB40AL Gene Mental Retardation X-Linked Genetic Test is 4400 AED. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory to identify any genetic mutations associated with the condition. The results of this test can provide valuable information for genetic counseling, helping families make informed decisions about future pregnancies and the management of the condition in affected family members.
The SLC9A6 gene mental retardation X-linked syndromic Christianson type genetic test is a specialized diagnostic assessment designed to identify mutations in the SLC9A6 gene, which are linked to Christianson syndrome. This condition, also known as X-linked Angelman syndrome, is a rare genetic disorder that affects neurological development, leading to intellectual disability, epilepsy, and difficulties with speech and movement. The test is crucial for early diagnosis and management of the syndrome, enabling tailored therapeutic strategies and support for affected individuals and their families.
Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient's DNA to detect specific mutations in the SLC9A6 gene that are associated with Christianson syndrome. The process is thorough, leveraging advanced genetic sequencing technologies to ensure accurate and reliable results.
The cost of the SLC9A6 gene mental retardation X-linked syndromic Christianson type genetic test is 4400 AED. While the price may seem significant, the value of obtaining a precise diagnosis cannot be understated, as it opens the door to specialized care and interventions that can significantly improve the quality of life for those affected by the condition.
The UBE2A gene mental retardation X-linked syndromic Nascimento-type genetic test is a specialized diagnostic tool designed to identify mutations in the UBE2A gene, which are linked to Nascimento syndrome. This condition is a rare form of X-linked intellectual disability that affects males and is characterized by features such as developmental delay, intellectual disability, sparse hair, distinctive facial features, and other physical abnormalities. The test is crucial for accurate diagnosis, allowing for tailored care and management plans for affected individuals.
Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves analyzing the patient's DNA to detect mutations in the UBE2A gene. Given the complexity of the test and the advanced technology employed, the cost is set at 4400 AED. This investment covers the comprehensive analysis required to ensure accurate results, providing essential information for families and healthcare providers in managing the condition and making informed decisions about care and support.
The ZDHHC9 Gene Mental Retardation X-Linked Syndromic Raymond Type Genetic Test is a specialized diagnostic procedure designed to identify mutations in the ZDHHC9 gene, which are linked to a rare form of X-linked mental retardation known as Raymond syndrome. This condition primarily affects males and is characterized by intellectual disability, speech and language delays, and sometimes physical abnormalities. The test involves analyzing the patient's DNA to detect any genetic anomalies that might be responsible for the syndrome.
Conducted at DNA Labs UAE, a leading facility in genetic testing and diagnostics, this test is essential for families seeking to understand the genetic basis of intellectual disabilities and related syndromes in their loved ones. It can also provide valuable information for genetic counseling and inform decisions regarding management and support for affected individuals.
The cost of the ZDHHC9 Gene Mental Retardation X-Linked Syndromic Raymond Type Genetic Test is 4400 AED. This investment covers the comprehensive analysis required to accurately identify the presence of genetic mutations associated with the condition. Given the complexity and specificity of the test, it represents a crucial step towards personalized care and intervention for those impacted by Raymond syndrome.
