The FIG4 Gene CMT4J Genetic Test is a specialized diagnostic tool designed to detect mutations in the FIG4 gene, which are linked to Charcot-Marie-Tooth disease type 4J (CMT4J). CMT4J is a rare and severe neurological disorder characterized by progressive weakness and atrophy of the muscles in the feet, hands, and elsewhere. The condition can also affect sensory nerves, leading to a loss of sensation in the affected areas.
This genetic test is crucial for individuals suspected of having CMT4J based on clinical symptoms or family history. Early and accurate diagnosis through the FIG4 Gene CMT4J Genetic Test allows for better management of the condition, including therapeutic interventions and genetic counseling for affected families.
The test is available at DNA Labs UAE, a leading facility in genetic testing and analysis. The cost of the test is 4400 AED. DNA Labs UAE utilizes state-of-the-art technology and adheres to the highest standards of accuracy and reliability in genetic diagnostics, ensuring that individuals receive comprehensive and precise information about their genetic health.
The GNB4 Gene CMTDIF Genetic Test is a specialized diagnostic procedure available at DNA Labs UAE, designed to detect mutations in the GNB4 gene, which are associated with Charcot-Marie-Tooth disease, type D, intermediate form (CMTDIF). Charcot-Marie-Tooth disease is a group of inherited disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems, primarily in the feet and legs, but also in the hands and arms in advanced stages.
The GNB4 gene plays a critical role in the normal functioning of nerve cells, and mutations in this gene can disrupt nerve signal transmission, leading to the symptoms observed in CMTDIF. The test is crucial for individuals with a family history of Charcot-Marie-Tooth disease or those exhibiting symptoms, as it provides a definitive diagnosis by identifying the specific genetic mutation responsible for the condition.
Performed at DNA Labs UAE, a leading facility in genetic testing, the GNB4 Gene CMTDIF Genetic Test involves collecting a DNA sample, usually through a blood draw or cheek swab. The sample is then analyzed using advanced genetic sequencing technologies to identify any mutations in the GNB4 gene.
The cost of the GNB4 Gene CMTDIF Genetic Test at DNA Labs UAE is 4400 AED. While the price may seem high, the test offers invaluable information for the management and treatment of Charcot-Marie-Tooth disease, potentially improving the quality of life for those affected by the condition. It also provides essential data for family planning and the assessment of risk for future generations.
The KARS1 Gene CMTRIB Genetic Test is a specialized diagnostic tool offered by DNA Labs UAE, designed to identify mutations in the KARS1 gene. These mutations are associated with Charcot-Marie-Tooth disease, recessive intermediate B (CMTRIB), a condition that affects the peripheral nerves. This genetic testing plays a crucial role in diagnosing the disorder, enabling healthcare providers to develop personalized treatment plans for affected individuals.
Priced at 4400 AED, the test involves analyzing the patient's DNA to detect any genetic alterations in the KARS1 gene that may lead to the development of CMTRIB. By pinpointing these mutations, the test provides valuable insights into the genetic basis of the disease, facilitating early intervention and management strategies. Conducted at the state-of-the-art facilities of DNA Labs UAE, this genetic test ensures accuracy and reliability, offering a critical resource for patients and families seeking answers to complex genetic conditions.
The COX6A1 gene CMTRID genetic test is a specialized diagnostic tool used to identify mutations in the COX6A1 gene, which can be associated with complex metabolic and neurological disorders. This test is crucial for individuals who may be exhibiting symptoms related to these conditions or have a family history of related genetic disorders. By analyzing the genetic material for specific mutations in the COX6A1 gene, healthcare providers can gain valuable insights into a patient's condition, enabling them to make more informed decisions regarding treatment and management.
The test is conducted at DNA Labs UAE, a reputable facility known for its advanced genetic testing capabilities and commitment to providing accurate and reliable results. The cost of the COX6A1 gene CMTRID genetic test is 4400 AED, an investment that can provide individuals and their families with essential information about their genetic health, potentially guiding therapeutic interventions and lifestyle adjustments to manage or mitigate the impact of the associated conditions.
The GJB1 gene CMTX1 genetic test is a specialized diagnostic tool used to identify mutations in the GJB1 gene, which are associated with Charcot-Marie-Tooth disease type X1 (CMTX1). CMTX1 is a form of Charcot-Marie-Tooth disease, a group of inherited disorders that affect the peripheral nerves, leading to muscle weakness and atrophy, as well as sensory loss. The GJB1 gene encodes a protein called connexin-32, which is crucial for the proper functioning of peripheral nerves.
The test is conducted through a blood sample or a cheek swab, which is then analyzed in a laboratory setting to detect any genetic abnormalities in the GJB1 gene. This genetic test is vital for the accurate diagnosis of CMTX1, allowing for appropriate management and treatment plans for affected individuals. It also provides essential information for family planning and genetic counseling for families with a history of Charcot-Marie-Tooth disease.
In the United Arab Emirates, this specific genetic test is available at DNA Labs UAE, a reputable facility known for its advanced genetic testing services. The cost of the GJB1 gene CMTX1 genetic test at DNA Labs UAE is 4400 AED. This cost includes the price of the test itself, as well as the professional services involved in the analysis and interpretation of the results. Patients seeking this test can expect a high standard of accuracy and confidentiality, along with comprehensive support throughout the testing process.
The AIFM1 gene CMTX4 genetic test is a specialized diagnostic tool designed to identify mutations in the AIFM1 gene, which are linked to Charcot-Marie-Tooth disease X-linked type 4 (CMTX4). CMTX4 is a rare form of Charcot-Marie-Tooth disease, a group of disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems primarily in the limbs. The AIFM1 gene plays a crucial role in maintaining mitochondrial function and its mutations can lead to various neurological symptoms associated with CMTX4.
This genetic test is particularly important for individuals showing symptoms of Charcot-Marie-Tooth disease or those with a family history of the disorder, as it can provide definitive diagnosis and help in the management and treatment planning. It is also valuable for at-risk family members for understanding their risk of developing or passing on the condition.
The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. The cost of the AIFM1 gene CMTX4 genetic test is 4400 AED. The process involves collecting a DNA sample, typically through a blood draw or a cheek swab, which is then analyzed in the laboratory to detect any mutations in the AIFM1 gene. Results from this test can offer crucial information for genetic counseling and guiding clinical management for affected individuals and their families.
The PRPS1 Gene CMTX5 Genetic Test is a specialized diagnostic tool designed to identify mutations in the PRPS1 gene, which are linked to Charcot-Marie-Tooth disease, type X5 (CMTX5). CMTX5 is a rare form of Charcot-Marie-Tooth disease, a genetic disorder that affects the peripheral nerves, leading to muscle weakness and sensory problems. The PRPS1 gene plays a crucial role in the synthesis of nucleotides, which are essential for DNA and RNA production. Mutations in this gene can disrupt nerve function, resulting in the symptoms associated with CMTX5.
This genetic test is available at DNA Labs UAE, a leading facility for genetic testing and analysis. The test is performed through a blood sample or a cheek swab, which is then analyzed for specific genetic alterations in the PRPS1 gene. The outcome of this test can provide valuable information for the diagnosis, treatment, and management of CMTX5, offering insights into potential therapeutic approaches and enabling families to understand their genetic risk for this condition.
The cost of the PRPS1 Gene CMTX5 Genetic Test at DNA Labs UAE is 4400 AED. This investment covers the comprehensive analysis required to accurately detect mutations in the PRPS1 gene, providing patients and healthcare providers with critical information for managing Charcot-Marie-Tooth disease, type X5.
The CC2D2A gene plays a critical role in the proper development and functioning of several body parts, including the brain and kidneys. Mutations in the CC2D2A gene are linked to COACH Syndrome, a rare genetic disorder characterized by Coloboma (a defect in the eye's iris or retina), Oligophrenia (developmental delays), Ataxia (lack of muscle coordination), Cerebellar hypoplasia (underdeveloped cerebellum), and Hepatic fibrosis (scarring of the liver).
To diagnose COACH Syndrome, a genetic test targeting the CC2D2A gene can be conducted. This test is crucial for confirming the diagnosis, understanding the severity of the condition, and guiding treatment and management decisions.
In the United Arab Emirates, DNA Labs UAE offers this specific genetic test for COACH Syndrome. The cost of the test is set at 4400 AED. DNA Labs UAE is known for its advanced genetic testing services, providing accurate and reliable results that are crucial for patients and their families dealing with genetic conditions like COACH Syndrome.
The RPGRIP1L gene plays a crucial role in the development and function of primary cilia, which are essential for cell signaling pathways. Mutations in the RPGRIP1L gene are associated with COACH Syndrome, a rare genetic disorder characterized by cerebellar vermis hypoplasia, oligophrenia (intellectual disability), ataxia, colobomas (defects in the iris or retina of the eye), and hepatic fibrosis. COACH Syndrome is part of a group of diseases known as ciliopathies, which are caused by dysfunction of the primary cilium.
To diagnose COACH Syndrome and identify the specific mutations in the RPGRIP1L gene, genetic testing is available at DNA Labs UAE. The test involves analyzing the patient's DNA to look for mutations in the RPGRIP1L gene that are known to cause the syndrome. This genetic test is critical for confirming the diagnosis, understanding the disease's progression, and guiding treatment and management decisions for affected individuals and their families.
The cost of the RPGRIP1L gene COACH Syndrome genetic test at DNA Labs UAE is 4400 AED. This comprehensive testing provides valuable information for the diagnosis and management of COACH Syndrome, facilitating personalized care plans and potentially improving outcomes for those affected by this rare condition.
The TMEM67 gene plays a crucial role in the proper development and function of various body systems. Mutations in this gene are associated with COACH syndrome, a rare genetic disorder characterized by a spectrum of clinical features including cerebellar vermis hypoplasia, oligophrenia (developmental delay), ataxia, coloboma, and hepatic fibrosis. Early diagnosis and intervention are crucial for managing the symptoms and improving the quality of life for affected individuals.
To assist in the diagnosis of COACH syndrome, DNA Labs UAE offers a genetic test specifically targeting the TMEM67 gene. This test is designed to detect mutations in the TMEM67 gene that are linked to the development of COACH syndrome. It is a vital tool for families with a history of the syndrome or for individuals presenting with symptoms suggestive of the condition.
The cost of the TMEM67 gene COACH syndrome genetic test at DNA Labs UAE is 4400 AED. The test involves a simple sample collection process, after which the sample is analyzed in the laboratory for the presence of specific genetic mutations in the TMEM67 gene. Results from this test can provide valuable information for the diagnosis, management, and genetic counseling of affected individuals and their families.
