The Chr. 15q11 Gene Angelman Syndrome Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the chromosome 15q11-q13 region, which are responsible for Angelman Syndrome. Angelman Syndrome is a genetic disorder that primarily affects the nervous system, leading to developmental delays, problems with speech and balance, intellectual disability, and sometimes, seizures. This condition is often caused by deletions or other genetic abnormalities in the maternal copy of the 15q11-q13 region.
The test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the lab for specific genetic changes associated with Angelman Syndrome. It is a critical tool for families seeking answers to developmental issues in their children, providing them with essential information for management and treatment strategies.
At DNA Labs UAE, the cost of the Chr. 15q11 Gene Angelman Syndrome Genetic Test is set at 3200 AED. The test is conducted with the utmost precision and care by experienced professionals, ensuring reliable and accurate results. DNA Labs UAE is equipped with state-of-the-art technology and follows stringent protocols to deliver high-quality genetic testing services.
The UBE3A Gene Angelman Syndrome Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, aimed at identifying mutations in the UBE3A gene, which are closely linked to Angelman syndrome. Angelman syndrome is a genetic disorder that primarily affects the nervous system, leading to developmental delays, problems with speech and balance, intellectual disability, and sometimes, seizures. This condition is often caused by the loss of function of the UBE3A gene located on chromosome 15.
DNA Labs UAE utilizes advanced genetic testing techniques to analyze the UBE3A gene for any abnormalities that might indicate the presence of Angelman syndrome. This test is crucial for early diagnosis and intervention, which can significantly improve the quality of life for individuals with this condition. The cost of the UBE3A Gene Angelman Syndrome Genetic Test is 4400 AED, reflecting the sophisticated nature of the genetic analysis and the invaluable insights it provides to affected families. Early diagnosis through this test can lead to better management strategies and support for individuals with Angelman syndrome and their families.
The MECP2 gene Angelman-like syndrome genetic test is a specialized diagnostic procedure aimed at identifying mutations in the MECP2 gene, which are associated with conditions resembling Angelman syndrome. Angelman-like syndromes are a group of neurodevelopmental disorders that share similar characteristics with Angelman syndrome but are caused by genetic abnormalities in different genes, including MECP2. Symptoms of these conditions can include developmental delays, speech impairments, seizures, and unique behaviors such as frequent laughter or smiling.
This test is particularly crucial for individuals showing symptoms of Angelman syndrome but without the typical genetic markers for that condition. By analyzing the MECP2 gene, healthcare professionals can accurately diagnose the presence of Angelman-like syndrome, enabling them to provide targeted interventions and support to patients and their families.
Conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing services, the MECP2 gene Angelman-like syndrome genetic test costs 4400 AED. The lab ensures precise and reliable results, thanks to its use of cutting-edge technology and adherence to stringent quality control measures. Opting for this test at DNA Labs UAE offers patients and healthcare providers a critical tool in the diagnosis and management of Angelman-like syndromes, paving the way for improved outcomes and quality of life for affected individuals.
The PRPS1 gene is associated with Arts syndrome, a rare genetic disorder characterized by various symptoms including sensorineural hearing loss, intellectual disability, and delayed development. The condition is inherited in an X-linked recessive pattern, meaning it predominantly affects males. The PRPS1 gene plays a crucial role in the synthesis of purine nucleotides, which are essential components of DNA and RNA. Mutations in the PRPS1 gene disrupt this synthesis, leading to the symptoms observed in Arts syndrome.
To diagnose this condition, a genetic test focusing on the PRPS1 gene can be conducted. In the UAE, DNA Labs offers this specialized genetic testing service. The test is designed to identify mutations in the PRPS1 gene that are indicative of Arts syndrome. It involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing the genetic material for specific mutations associated with the syndrome.
The cost of the PRPS1 Gene Arts syndrome Genetic Test at DNA Labs UAE is 4400 AED. This price may cover the genetic testing process, analysis, and reporting. Receiving a diagnosis through this test can be crucial for affected individuals and their families, as it provides a clear understanding of the condition and can guide treatment and management decisions. It is always recommended to consult with a healthcare professional or genetic counselor before and after undergoing genetic testing to ensure a comprehensive understanding of the test results and their implications.
The NLGN3 Gene Asperger Syndrome Susceptibility X-Linked Type 2 Genetic Test is a specialized diagnostic tool designed to assess the risk of developing Asperger Syndrome, a condition on the autism spectrum that affects communication and social interaction skills. This test specifically investigates the NLGN3 gene, which has been linked to the susceptibility of Asperger Syndrome and is located on the X chromosome, indicating that it could have a distinct pattern of inheritance. Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the individual's DNA to identify any mutations or alterations in the NLGN3 gene that could increase the likelihood of developing Asperger Syndrome.
The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to accurately analyze genetic information and provide meaningful insights. This test is crucial for families with a history of Asperger Syndrome or related conditions, as it can offer early identification of the syndrome's risk, allowing for prompt intervention and support strategies. By understanding an individual's genetic predisposition, healthcare providers can tailor their approach to meet specific needs, improving the quality of life for those affected by Asperger Syndrome.
The "COX20 Gene Ataxia and Muscle Hypotonia Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the COX20 gene, which are associated with certain neurodegenerative disorders. Ataxia, characterized by a lack of muscle control during voluntary movements, and muscle hypotonia, a condition marked by reduced muscle tone, can both result from anomalies in the COX20 gene. This gene plays a crucial role in the proper functioning of the mitochondria, the powerhouse of the cell, and its mutations can lead to a variety of mitochondrial disorders.
The test, priced at 4400 AED, involves collecting a DNA sample from the patient, typically through a blood draw or a cheek swab. The genetic material is then analyzed using advanced sequencing technologies to identify any mutations in the COX20 gene. Results from this test can provide crucial information for the diagnosis, management, and treatment planning for individuals exhibiting symptoms of ataxia and muscle hypotonia, potentially guiding families towards appropriate genetic counseling and support services. DNA Labs UAE ensures confidentiality and accuracy in the testing process, offering a comprehensive approach to understanding genetic contributions to these complex conditions.
The ALS2 gene amyotrophic lateral sclerosis type 2 juvenile genetic test is a specialized diagnostic tool aimed at identifying mutations in the ALS2 gene, which are linked to the development of juvenile amyotrophic lateral sclerosis (ALS) type 2. This form of ALS is an inherited neurodegenerative disorder that affects motor neurons, leading to progressive muscle weakness and atrophy. The onset of symptoms typically occurs in childhood or adolescence, making early diagnosis crucial for managing the condition and planning appropriate care.
DNA Labs UAE offers this genetic test, providing a comprehensive analysis of the ALS2 gene to detect mutations that could indicate a predisposition to developing ALS type 2. The test is performed using a sample of the patient's blood or saliva, which is then analyzed using advanced genetic sequencing techniques to identify any genetic alterations.
The cost of the ALS2 gene amyotrophic lateral sclerosis type 2 juvenile genetic test at DNA Labs UAE is 4400 AED. This price reflects the intricate nature of genetic testing and the specialized expertise required to accurately interpret the results. Individuals considering this test are often those with a family history of ALS type 2 or early signs of the disease, aiming to confirm a diagnosis and explore potential treatment or management strategies.
By opting for this test at DNA Labs UAE, patients and their families can gain valuable insights into their genetic makeup, empowering them with information that could significantly impact their approach to managing juvenile ALS type 2.
The MATR3 Gene Amyotrophic Lateral Sclerosis Type 21 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the MATR3 gene, which are associated with the development of Amyotrophic Lateral Sclerosis (ALS) type 21. ALS, also known as Lou Gehrig's disease, is a progressive neurodegenerative disorder that affects nerve cells in the brain and the spinal cord, leading to muscle weakness and, eventually, severe physical disability.
The test is particularly crucial for individuals with a family history of ALS or symptoms indicative of the disease, as identifying the genetic mutation can help in understanding the risk, potential progression, and possible familial implications of the condition. Conducted at DNA Labs UAE, a leading facility in genetic testing and diagnostics, the test ensures accuracy and confidentiality in handling patient samples.
The cost of the MATR3 Gene Amyotrophic Lateral Sclerosis Type 21 Genetic Test is 4400 AED. This investment covers the genetic analysis and the expertise required to interpret the results accurately. Given the complexity and the specialized nature of the test, the cost reflects the comprehensive analysis and detailed report provided to the patient, which can be instrumental in planning for treatment and management of the condition.
It's important for patients considering this test to consult with a healthcare provider or a genetic counselor to fully understand the implications of the results and to ensure that it is the right step in their diagnostic journey.
The FUS Gene Amyotrophic Lateral Sclerosis Type 6 Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to identify mutations in the FUS gene, which are associated with the development of Amyotrophic Lateral Sclerosis (ALS) type 6. ALS, also known as Lou Gehrig's disease, is a progressive neurodegenerative disorder that affects nerve cells in the brain and the spinal cord, leading to muscle weakness and, eventually, severe physical disability. The FUS gene plays a critical role in the functioning of neurons, and mutations in this gene can lead to the familial form of ALS, which accounts for a small percentage of ALS cases.
This test is particularly important for individuals with a family history of ALS or those who have been diagnosed with ALS and are seeking a genetic explanation for their condition. By identifying the presence of FUS gene mutations, the test can provide crucial information for the diagnosis, prognosis, and potential treatment options for patients and their families. It can also aid in genetic counseling for family members who may be at risk.
The cost of the FUS Gene Amyotrophic Lateral Sclerosis Type 6 Genetic Test at DNA Labs UAE is 4400 AED. The test is conducted using a sample of the patient's blood or saliva, which is then analyzed in the laboratory for the presence of genetic mutations in the FUS gene. The results of this test can have significant implications for the management and understanding of ALS, making it a valuable tool in the fight against this challenging condition.
The VAPB Gene Amyotrophic Lateral Sclerosis type 8 Genetic Test is a specialized diagnostic procedure designed to identify mutations in the VAPB gene, which have been associated with a rare form of Amyotrophic Lateral Sclerosis (ALS), also known as ALS type 8. This condition is a progressive neurodegenerative disorder that affects nerve cells in the brain and the spinal cord, leading to muscle weakness and, eventually, severe physical disability.
The test is conducted at DNA Labs UAE, a leading facility in genetic testing and analysis. By examining a patient's DNA sample, usually obtained through a blood draw, the test can pinpoint specific genetic alterations in the VAPB gene that are indicative of ALS type 8. This information is crucial for early diagnosis, allowing for better management of the condition and counseling for affected individuals and their families.
The cost of the VAPB Gene Amyotrophic Lateral Sclerosis type 8 Genetic Test at DNA Labs UAE is 4400 AED. This price includes the full analysis and a comprehensive report that details the findings. Given the complexity of genetic testing and the specialized technology required, the cost reflects the extensive resources involved in providing accurate and reliable results.
