The F5 Gene Budd-Chiari Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the F5 gene, which have been associated with an increased risk of Budd-Chiari Syndrome (BCS). BCS is a rare vascular disorder characterized by the obstruction of the hepatic veins, which can lead to liver damage, and in severe cases, liver failure. The condition is complex, with genetic factors playing a crucial role in its development alongside environmental influences.
This genetic test is crucial for individuals with a family history of BCS or those exhibiting symptoms related to liver dysfunction, as it can provide valuable insights into their risk of developing this condition. Early detection through genetic testing allows for timely intervention and management strategies to mitigate the risk of severe complications associated with BCS.
The test is conducted at DNA Labs UAE, a state-of-the-art facility known for its advanced genetic testing services. The cost of the F5 Gene Budd-Chiari Syndrome Genetic Test is 4400 AED. Given the specialized nature of this test and its potential to significantly impact patient care, it represents a valuable investment in one's health, particularly for those at increased risk of this syndrome.
The ASPA Gene Canavan Disease Genetic Test is a specialized diagnostic tool used to identify mutations in the ASPA gene, which are responsible for Canavan disease. Canavan disease is a rare inherited disorder that causes progressive damage to nerve cells in the brain. This condition is particularly prevalent in individuals of Ashkenazi Jewish descent, but it can affect people from any ethnic background.
The test is conducted by extracting a DNA sample, typically through a blood draw or cheek swab, and analyzing it for specific genetic mutations in the ASPA gene. These mutations lead to a deficiency in the enzyme aspartoacylase, which is crucial for maintaining healthy brain tissue. The absence or malfunction of this enzyme results in the accumulation of N-acetylaspartic acid (NAA) in the brain, causing the progressive neurological symptoms observed in Canavan disease.
Offered by DNA Labs UAE, the ASPA Gene Canavan Disease Genetic Test is available for a cost of 4400 AED. DNA Labs UAE is a reputable facility known for its state-of-the-art genetic testing services. The test provides crucial information for prospective parents with a family history of Canavan disease, individuals of Ashkenazi Jewish heritage, or parents of children showing symptoms related to the disease. Early diagnosis through this genetic test can aid in management and treatment planning, although there is currently no cure for Canavan disease. The test is also an essential tool for carrier screening, allowing individuals to understand their carrier status and assess the risk of passing the condition onto their children.
The EIF4E Gene Autism Susceptibility Type 19 Genetic Test is a specialized diagnostic tool designed to identify genetic variations in the EIF4E gene, which have been associated with an increased risk of developing autism spectrum disorder (ASD). This test plays a crucial role in understanding the genetic underpinnings of ASD, particularly in cases where the EIF4E gene is implicated. By analyzing the DNA sequence of the EIF4E gene, this test can detect mutations that may contribute to the condition, providing valuable information for families and healthcare providers.
Conducted at DNA Labs UAE, a leading facility in genetic testing and analysis, the test ensures accuracy and reliability in its results. The cost of the test is set at 4400 AED, reflecting the comprehensive nature of the analysis and the sophisticated technology employed. This test is a significant step forward in personalized medicine, offering insights that can guide interventions and support for individuals with ASD and their families.
The "NLGN3 Gene Autism Susceptibility X-Linked Type 1 Genetic Test" is a specialized diagnostic tool designed to identify mutations in the NLGN3 gene, which is linked to the development of autism spectrum disorder (ASD), particularly in a form that is inherited in an X-linked pattern. This means that the gene responsible for this condition is located on the X chromosome, one of the two sex chromosomes, making it more commonly observed in males who have only one X chromosome.
Autism spectrum disorder is a complex developmental condition that involves persistent challenges in social interaction, speech and nonverbal communication, and restricted/repetitive behaviors. The role of the NLGN3 gene in autism has been a subject of research, as mutations in this gene can affect brain function and development, leading to symptoms associated with ASD.
The test offered by DNA Labs UAE utilizes advanced genetic sequencing techniques to analyze the NLGN3 gene for any abnormalities that might be associated with an increased risk of developing autism. By identifying these mutations, the test can provide valuable information for families with a history of ASD, offering insights into the genetic underpinnings of the disorder and aiding in the early diagnosis and management of affected individuals.
Priced at 4400 AED, this genetic test is a significant investment in understanding the genetic factors contributing to autism susceptibility. It is particularly relevant for individuals or families with a history of X-linked disorders or those seeking a deeper understanding of their genetic health. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, clients can expect professional handling of their samples and accurate, confidential results.
The "SHANK2 Gene Autism Susceptibility X-Linked Type 17 Genetic Test" is a specialized diagnostic tool designed to identify mutations in the SHANK2 gene, which have been linked to an increased risk of autism spectrum disorders (ASD). This genetic test is crucial for individuals with a family history of autism or those showing symptoms of ASD, as it can provide a clearer understanding of their condition and guide potential treatment and management strategies.
Performed at DNA Labs UAE, a leading facility in genetic testing and analysis, this test involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab. The sample is then analyzed to detect any abnormalities or mutations in the SHANK2 gene that are associated with autism susceptibility X-linked type 17, a specific subtype of autism that has a genetic basis.
The cost of the SHANK2 Gene Autism Susceptibility X-Linked Type 17 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 SHANK2 gene. While the cost may seem high, the value of the insights gained from this test can be invaluable for affected individuals and their families, offering a path towards more personalized and effective approaches to managing autism spectrum disorders.
The NLGN4X Gene Autism Susceptibility X-Linked Type 2 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the NLGN4X gene, which is linked to a susceptibility to autism spectrum disorder (ASD) specifically in a pattern that suggests X-linked inheritance. This test is crucial for families with a history of ASD or for individuals showing symptoms of autism, as it can provide essential insights into the genetic underpinnings of the condition. By analyzing DNA samples, the test can detect variations in the NLGN4X gene that are associated with an increased risk of developing ASD, thereby facilitating early intervention and personalized management strategies. The cost of the test is 4400 AED, reflecting the specialized nature of the genetic analysis and the comprehensive support provided by DNA Labs UAE in interpreting the results and guiding subsequent steps for individuals and families.
The "MECP2 Gene Autism Susceptibility X-Linked Type 3 Genetic Test" is a specialized diagnostic tool offered by DNA Labs UAE, aimed at identifying mutations in the MECP2 gene, which have been linked to a higher susceptibility to autism, particularly in a form that is X-linked. This form of testing is crucial for early detection and intervention in individuals who may be at risk for developing autism spectrum disorders (ASDs) due to genetic predispositions. The MECP2 gene plays a significant role in the development of the nervous system, and mutations in this gene can lead to various neurological disorders, including certain types of autism.
The test, priced at 4400 AED, involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific genetic variations in the MECP2 gene that are associated with an increased risk of autism. This information can be invaluable for families with a history of autism or related disorders, providing them with early insights and the possibility to engage in early intervention strategies that can significantly improve the quality of life for those affected. DNA Labs UAE, with its state-of-the-art facilities and expert geneticists, ensures high accuracy and reliability of the test results, making it a trusted choice for genetic testing related to autism susceptibility.
The TMLHE Gene Autism Susceptibility X-Linked Type 6 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the TMLHE gene that have been linked to an increased risk of autism spectrum disorder (ASD) in a sex-linked manner. This gene plays a crucial role in the biosynthesis of carnitine, a substance essential for the metabolism of fatty acids in the mitochondria. Alterations or mutations in the TMLHE gene can disrupt this process, potentially contributing to the development of ASD.
The test is priced at 4400 AED and involves collecting a DNA sample from the patient, typically through a blood draw or cheek swab. The sample is then analyzed using advanced genetic sequencing technologies to identify any mutations in the TMLHE gene. This information can be invaluable for families with a history of ASD, providing insights into the genetic underpinnings of the disorder and aiding in early diagnosis and intervention strategies.
DNA Labs UAE, where this test is conducted, is equipped with state-of-the-art facilities and staffed by experts in genetic testing and counseling. They ensure that the testing process is conducted with the utmost precision and care, providing patients and their families with reliable results and comprehensive support throughout the diagnostic journey.
The ATP1B4 gene, associated with the ATPase Na+/K+ transporting family, has garnered attention in the realm of autism research due to its potential link to the condition. Autism spectrum disorder (ASD) is a complex developmental disorder characterized by difficulties with social interaction, communication challenges, and a tendency to engage in repetitive behaviors. The exploration into genetic components like the ATP1B4 gene aims to unravel the intricate biological underpinnings of autism, offering insights that could lead to more targeted interventions and therapies.
DNA Labs UAE, a leading facility in genetic testing, offers a comprehensive ATP1B4-related genetic test designed to identify variations in the ATP1B4 gene that may be associated with autism. This test is a crucial tool for researchers and healthcare providers in understanding the genetic landscape of individuals with ASD, potentially leading to personalized treatment plans that address the specific needs of each patient.
The test is priced at 4400 AED, reflecting the advanced technology and expertise required to conduct such sophisticated genetic analyses. By opting for this test at DNA Labs UAE, individuals can gain valuable insights into their genetic makeup, providing a foundation for informed healthcare decisions and a proactive approach to managing conditions like autism.
The C7orf43 gene, located on chromosome 7, has recently been identified as a potential marker in the genetic testing for autism spectrum disorder (ASD). Research indicates that variations in the C7orf43 gene may contribute to the development of ASD, making it a significant focus for genetic testing aimed at early diagnosis and intervention.
DNA Labs UAE offers a specialized genetic test targeting the C7orf43 gene to assess the risk of ASD. This test is particularly valuable for families with a history of autism or related disorders, as it provides crucial insights into genetic predispositions. By analyzing specific markers within the C7orf43 gene, DNA Labs UAE can identify variations that are associated with an increased risk of ASD.
The test is priced at 4400 AED and involves a simple, non-invasive procedure. Results from the test can guide families and healthcare professionals in developing personalized management plans for children at risk, potentially improving outcomes through early intervention strategies. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in the field of genetic testing, ensuring reliable and accurate results for those seeking insights into ASD risk related to the C7orf43 gene.
