The NTRK1 gene HSAN4 genetic test is a specialized diagnostic tool used to detect mutations in the NTRK1 gene, which are associated with Hereditary Sensory and Autonomic Neuropathy Type IV (HSAN4), also known as Congenital Insensitivity to Pain with Anhidrosis (CIPA). This condition is characterized by the inability to feel pain and temperature, leading to repeated injuries and infections. Additionally, individuals with HSAN4 may not sweat (anhidrosis), which can cause overheating.
The test involves analyzing the patient's DNA to identify any genetic abnormalities in the NTRK1 gene that could lead to the development of HSAN4. Early diagnosis through this genetic test can aid in the management of the condition and help in taking preventive measures against potential complications.
The cost of the NTRK1 gene HSAN4 genetic test is 4400 AED. The test is conducted at DNA Labs UAE, a leading facility that specializes in providing comprehensive genetic testing services. DNA Labs UAE employs advanced technology and follows strict protocols to ensure accurate and reliable results, making it a trusted choice for genetic testing in the region.
The NGF Gene HSAN5 Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the NGF gene, which are associated with Hereditary Sensory and Autonomic Neuropathy Type 5 (HSAN5). HSAN5 is a rare genetic disorder characterized by an insensitivity to pain, anhidrosis (inability to sweat), and various other sensory impairments. The test plays a crucial role in the early detection and management of this condition, providing essential information for healthcare providers to develop appropriate treatment plans.
Performed at the state-of-the-art facilities of DNA Labs UAE, the test requires a DNA sample, usually collected through a simple and non-invasive method such as a saliva swab or blood sample. The laboratory employs advanced genetic sequencing technologies to analyze the NGF gene for any mutations that could indicate the presence of HSAN5.
The cost of the NGF Gene HSAN5 Genetic Test at DNA Labs UAE is set at 4400 AED. While the price may seem significant, the value of the information it provides for affected individuals and their families cannot be overstated. Early diagnosis through this test can lead to better management of symptoms, improved quality of life, and informed genetic counseling for families.
Individuals considering this test are advised to consult with a healthcare professional or genetic counselor to discuss its implications fully and to understand how the results may impact their health and lifestyle decisions.
The PRDM12 Gene HSAN8 Genetic Test is a specialized diagnostic tool designed to detect mutations in the PRDM12 gene, which are associated with Hereditary Sensory and Autonomic Neuropathy Type VIII (HSAN8). HSAN8 is a rare genetic disorder characterized by severe pain insensitivity, inability to sweat, and other sensory and autonomic nervous system dysfunctions. The test aims to provide crucial information for the accurate diagnosis of HSAN8, enabling appropriate management and counseling for affected individuals and their families.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves analyzing the patient's DNA to identify mutations in the PRDM12 gene. This comprehensive analysis helps in confirming the diagnosis of HSAN8, which is essential for guiding treatment decisions and offering genetic counseling. The cost of the PRDM12 Gene HSAN8 Genetic Test is 4400 AED, reflecting the intricate technology and expertise required to accurately identify the genetic variations associated with this condition.
The KIF1A Gene HSN2C Genetic Test is a specialized diagnostic examination offered by DNA Labs UAE, designed to identify mutations in the KIF1A gene that are associated with Hereditary Sensory and Autonomic Neuropathy Type 2C (HSN2C). This condition is a rare genetic disorder that affects the peripheral nervous system, leading to sensory loss, muscle weakness, and autonomic dysfunction. The test is critical for individuals who exhibit symptoms suggestive of HSN2C or have a family history of the condition, as early detection can significantly impact management and treatment strategies.
Performed in the state-of-the-art facilities of DNA Labs UAE, the test involves analyzing the patient's DNA sample to search for specific genetic alterations in the KIF1A gene that are known to cause HSN2C. The process is highly accurate and provides essential information for genetic counseling, guiding treatment decisions, and assessing the risk of passing the condition to future generations.
The cost of the KIF1A Gene HSN2C 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 KIF1A gene. For patients and families dealing with the possibility of HSN2C, this test represents a critical step towards understanding their genetic health and making informed decisions about their care.
The HTT Gene Huntington Disease Genetic Test is a specialized diagnostic procedure designed to identify mutations in the HTT gene, which are responsible for Huntington's disease (HD). Huntington's disease is a progressive brain disorder that affects movement, cognition, and can cause psychiatric disorders. The test is crucial for individuals with a family history of Huntington's disease or those displaying symptoms, as it provides a definitive diagnosis and helps in planning the appropriate management and treatment strategies.
Performed at DNA Labs UAE, a leading facility in genetic testing, the test involves collecting a DNA sample, typically through a blood draw or cheek swab. The laboratory then analyzes the HTT gene for specific mutations known to cause Huntington's disease. The focus is on the number of CAG repeats in the gene, as an increased number is directly linked to the development and severity of the disease.
The cost of the HTT Gene Huntington Disease Genetic Test at DNA Labs UAE is 4400 AED. While the price might seem steep, the test offers invaluable information for affected individuals and their families, enabling them to make informed decisions about their health and future. It is recommended to consult with a genetic counselor both before and after the test to fully understand the implications of the results and to receive support in dealing with the outcomes.
The ZDHHC17 gene, also known as Huntington Interacting Protein 14 (HIP14), plays a crucial role in the neuropathology of Huntington's Disease (HD), a progressive brain disorder that affects movement, behavior, and cognition. The ZDHHC17 gene encodes an enzyme involved in palmitoylation, a post-translational modification essential for the proper functioning and localization of proteins within cells. Mutations or dysfunctions in this gene have been linked to the development and progression of Huntington's Disease, making it a significant focus for genetic testing and research.
Genetic testing for Huntington's Disease related to the ZDHHC17 gene provides critical information for individuals with a family history of the disease or those showing symptoms, enabling them to make informed decisions about their health and future. The test typically involves analyzing DNA to identify mutations in the ZDHHC17 gene that might increase the risk or confirm the diagnosis of Huntington's Disease.
In the United Arab Emirates, DNA Labs UAE offers this specialized genetic test for individuals concerned about their risk of Huntington's Disease. The test cost is set at 4400 AED, reflecting the comprehensive analysis and detailed report provided by the lab. Conducting the test at DNA Labs UAE ensures that individuals receive accurate and reliable results, benefiting from the lab's expertise in genetic diagnostics and its use of advanced testing technologies. This service not only aids in early diagnosis and intervention but also supports families in understanding their genetic health, potentially guiding them towards appropriate counseling and management strategies for Huntington's Disease.
The PRNP Gene Huntington Disease-like Type 1 Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the PRNP gene associated with Huntington Disease-like 1 (HDL1). HDL1 is a rare neurodegenerative disorder that shares clinical features with Huntington's disease, including movement disorders, psychiatric symptoms, and cognitive decline, but is caused by different genetic abnormalities. This particular test focuses on identifying the specific mutations in the PRNP gene, which is critical for accurate diagnosis and differentiation from other similar conditions.
Priced at 4400 AED, the test is conducted in the state-of-the-art facilities of DNA Labs UAE, where advanced genetic testing technologies are utilized to ensure high accuracy and reliability of the results. This test is crucial for families with a history of HDL1, as it not only aids in confirming the diagnosis but also helps in understanding the risk of passing the mutation to the next generation. Early and precise diagnosis through the PRNP Gene Huntington Disease-like Type 1 Genetic Test can significantly impact the management and treatment strategies for affected individuals, providing them with a better quality of life.
The JPH3 gene Huntington Disease-like Type 2 genetic test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the JPH3 gene, which are associated with Huntington Disease-like 2 (HDL2). HDL2 is a rare neurodegenerative disorder that shares many clinical features with Huntington's disease, including movement disorders, psychiatric disturbances, and cognitive decline. The condition is inherited in an autosomal dominant pattern, meaning a mutation in just one of the two copies of the JPH3 gene can lead to the disease.
This test is crucial for individuals with a family history of HDL2 or those exhibiting symptoms suggestive of Huntington's disease but who have tested negative for the more common HTT gene mutation associated with Huntington's. Early and accurate diagnosis through the JPH3 gene test can facilitate better management of the condition, allow for genetic counseling, and inform family planning decisions.
The test is conducted at DNA Labs UAE, a facility renowned for its state-of-the-art genetic testing services. The cost of the test is set at 4400 AED, reflecting the specialized nature of the analysis and the expertise required to interpret the results accurately. By opting for this test, patients and their families can gain valuable insights into their genetic status and take proactive steps in managing their health.
The ARX gene, known for its pivotal role in brain development and function, has been linked to a range of neurological disorders, including Hydranencephaly with Abnormal Genitalia and Lissencephaly X-Linked 2. These conditions are characterized by severe brain malformations and, in some cases, abnormalities in genital development. Hydranencephaly involves the replacement of the brain's cerebral hemispheres with sacs filled with cerebrospinal fluid, while Lissencephaly X-Linked 2 is marked by a "smooth brain" due to abnormal neuronal migration, leading to intellectual disability and seizures.
To diagnose these conditions, genetic testing targeting the ARX gene can be instrumental. DNA Labs UAE offers a specialized genetic test for this purpose. The test aims to identify mutations in the ARX gene that are indicative of these disorders, providing crucial information for diagnosis, treatment planning, and genetic counseling. The cost of the test is 4400 AED, reflecting the sophisticated technology and expertise required to conduct such specialized genetic analysis. By opting for this test, individuals can gain valuable insights into their genetic makeup, empowering them with information that can guide medical and personal decision-making.
The "L1CAM Gene Hydrocephalus with Aqueductal Stenosis and Congenital Intestinal Pseudoobstruction Genetic Test" is a specialized diagnostic examination offered by DNA Labs UAE, designed to detect mutations in the L1CAM gene. These mutations are linked to a spectrum of severe conditions including hydrocephalus, characterized by the accumulation of cerebrospinal fluid in the brain due to aqueductal stenosis (a narrowing of the brain's aqueduct of Sylvius), and congenital intestinal pseudo-obstruction, a severe disorder affecting the normal movements of the intestines. The test, priced at 4400 AED, is crucial for early diagnosis and management, guiding treatment plans and genetic counseling for affected families. It involves collecting a DNA sample, usually through a blood draw, and analyzing it for specific genetic alterations in the L1CAM gene, providing insights into the risk and presence of these complex conditions.
