The "FLNA Gene Heterotopia Periventricular ED Variant Genetic Test" is a specialized diagnostic tool offered by DNA Labs UAE, designed to detect mutations in the FLNA gene, which are associated with periventricular nodular heterotopia (PVNH). PVNH is a neurological disorder characterized by the presence of nodules of neurons in inappropriate locations in the brain due to their failure to migrate to their correct positions during early brain development. This condition can lead to a variety of symptoms, including seizures, developmental delay, and coordination problems.
The FLNA gene plays a crucial role in cell structure and movement, and mutations in this gene can disrupt the normal neuronal migration process. The "ED Variant" in the test name refers to a specific variant of the condition that may have distinct genetic characteristics or clinical manifestations.
Offered at a cost of 4400 AED, this genetic test involves analyzing the patient's DNA to identify mutations in the FLNA gene that are indicative of periventricular nodular heterotopia. The test is crucial for accurate diagnosis, allowing for personalized treatment plans that can improve patient outcomes. Conducted at DNA Labs UAE, a facility known for its advanced genetic testing capabilities, this test represents a vital resource for individuals exhibiting symptoms of PVNH or those with a family history of the condition, enabling early intervention and management of the disorder.
The FLNA Gene Heterotopia Periventricular X-Linked Dominant Genetic Test is a specialized diagnostic assessment designed to identify mutations in the FLNA gene, which are associated with X-linked periventricular heterotopia (PVNH). This condition is characterized by the abnormal localization of neurons in the brain, leading to a range of neurological symptoms, including epilepsy, developmental delays, and sometimes, issues with coordination and muscle tone. Given the X-linked dominant inheritance pattern, mutations in the FLNA gene can significantly impact both males and females, though the severity and presentation can vary widely.
Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, this test aims to provide crucial information for the diagnosis and management of individuals suspected of having PVNH. The process involves collecting a DNA sample, typically through a blood draw, which is then analyzed for specific mutations in the FLNA gene that are indicative of the disorder.
The cost of the FLNA Gene Heterotopia Periventricular X-Linked Dominant Genetic Test is 4400 AED. This price reflects the comprehensive nature of the test, encompassing the sophisticated techniques used to detect gene mutations, as well as the expertise required to interpret the results accurately. For families affected by neurological conditions or for individuals showing symptoms related to PVNH, this test offers a valuable tool for understanding the genetic basis of the condition and guiding treatment and management decisions.
The RNF39 gene is implicated in various neurological functions, including the process of hippocampal long-term potentiation (LTP), which is fundamental for learning and memory. The RNF39-related genetic test is a specialized diagnostic tool designed to identify mutations or alterations in the RNF39 gene that may affect cognitive functions and neurological health. This test is particularly relevant for individuals experiencing cognitive impairments, memory issues, or other neurological symptoms that could be linked to genetic abnormalities affecting hippocampal LTP.
Conducted at DNA Labs UAE, a leading facility in genetic diagnostics, the test offers a comprehensive analysis of the RNF39 gene. The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately identify and interpret genetic variations. By undergoing this test, individuals can gain valuable insights into their genetic makeup, potentially leading to personalized treatment plans or interventions to address any identified issues. DNA Labs UAE ensures confidentiality and provides detailed consultations to help individuals understand their results and the implications for their health and well-being.
The DKC1 gene plays a pivotal role in the diagnosis of Hoyeraal-Hreidarsson Syndrome (HHS), a rare and severe variant of Dyskeratosis Congenita. This condition is characterized by multisystem abnormalities, including bone marrow failure, immunodeficiency, and developmental defects. The genetic test for the DKC1 gene specifically targets mutations associated with HHS, offering crucial insights for accurate diagnosis and management of the syndrome.
Performed at DNA Labs UAE, this genetic test is priced at 4400 AED. The laboratory utilizes advanced genomic technologies to ensure precise and reliable detection of mutations within the DKC1 gene. This test is not only vital for confirming the diagnosis of Hoyeraal-Hreidarsson Syndrome but also plays a significant role in guiding treatment decisions, understanding prognosis, and facilitating genetic counseling for affected families. With a focus on accuracy and comprehensive care, DNA Labs UAE stands as a premier facility for genetic testing services in the region.
The SPTLC1 gene is associated with Hereditary Sensory and Autonomic Neuropathy Type I (HSAN1), a rare genetic disorder characterized by loss of sensation and muscle weakness. The SPTLC1 gene plays a crucial role in the biosynthesis of sphingolipids, which are essential components of cell membranes and involved in various cellular functions. Mutations in the SPTLC1 gene lead to the accumulation of toxic substances in nerve cells, causing the symptoms associated with HSAN1.
To diagnose HSAN1, a genetic test targeting the SPTLC1 gene can be conducted. This test is designed to identify mutations in the SPTLC1 gene that are responsible for the disorder. Early diagnosis through genetic testing can facilitate better management of the condition and help in understanding the risk of passing the disorder to future generations.
In the United Arab Emirates, the SPTLC1 gene HSAN1 genetic test is available at DNA Labs UAE. The cost of the test is 4400 AED. DNA Labs UAE is equipped with state-of-the-art technology to provide accurate and reliable genetic testing services. By opting for this test at DNA Labs UAE, individuals suspected of having HSAN1 or those with a family history of the disorder can gain valuable insights into their genetic makeup, enabling informed decisions regarding their health and the health of their family members.
The WNK1 Gene HSAN2A Genetic Test is a specialized diagnostic assessment available at DNA Labs UAE, designed to identify mutations in the WNK1 gene, which are linked to Hereditary Sensory and Autonomic Neuropathy Type II (HSAN2A). HSAN2A is a rare genetic disorder characterized by severe impairment of sensory and autonomic nervous system functions, leading to symptoms like loss of pain and temperature sensations, wound-healing issues, and autonomic dysregulation affecting sweating and blood pressure.
This test is crucial for individuals showing symptoms of HSAN2A, as it helps in confirming the diagnosis, understanding the disease progression, and making informed decisions regarding management and treatment options. The test involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the state-of-the-art facilities of DNA Labs UAE.
The cost of the WNK1 Gene HSAN2A Genetic Test at DNA Labs UAE is set at 4400 AED. Given the complexity of the test and the specialized analysis required, this cost reflects the extensive resources utilized in providing accurate and reliable results. Undergoing this test at DNA Labs UAE ensures access to cutting-edge genetic testing technology, expert analysis, and comprehensive support, making it a valuable tool for affected individuals and their families in managing HSAN2A.
The RETREG1 Gene HSAN2B Genetic Test is a specialized diagnostic tool designed to identify mutations in the RETREG1 gene, which are linked to Hereditary Sensory and Autonomic Neuropathy Type II (HSAN2B). HSAN2B is a rare genetic disorder characterized by severe impairment of sensory and autonomic nervous system functions, leading to symptoms such as loss of pain and temperature sensation, wound-healing issues, and autonomic dysfunctions. This test is crucial for individuals displaying symptoms of HSAN2B or those with a family history of the condition, as it can provide a definitive diagnosis, guiding treatment and management strategies.
Performed at DNA Labs UAE, a leading facility in genetic diagnostics, the test involves collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed for specific mutations in the RETREG1 gene. The cost of the RETREG1 Gene HSAN2B Genetic Test is 4400 AED, reflecting the specialized nature of the testing and the comprehensive analysis it entails. This investment is valuable for affected individuals and their families, as it not only confirms the diagnosis but also assists in genetic counseling and the evaluation of potential risks to other family members.
The ELP1 gene HSAN3 genetic test is a specialized diagnostic procedure designed to identify mutations in the ELP1 gene, which are associated with Hereditary Sensory and Autonomic Neuropathy Type III (HSAN3), also known as Familial Dysautonomia. This condition is a rare genetic disorder characterized by sensory and autonomic nervous system dysfunction, leading to a wide range of symptoms such as insensitivity to pain, temperature regulation issues, and blood pressure instability.
The test is conducted at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The procedure involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed in the laboratory to detect any genetic abnormalities in the ELP1 gene.
The cost of the ELP1 gene HSAN3 genetic test at DNA Labs UAE is set at 4400 AED. This price includes the full process of sample collection, analysis, and the provision of a detailed report explaining the test results. The report is crucial for understanding the individual's genetic risk for developing HSAN3 and can inform clinical management and genetic counseling for the individual and their family.
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.
