The RAB7A Gene CMT2B Genetic Test is a specialized diagnostic tool designed to identify mutations in the RAB7A gene, which are associated with Charcot-Marie-Tooth disease type 2B (CMT2B). CMT2B 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 feet and legs, sometimes affecting the hands and arms in the advanced stages of the disease.
This test is crucial for patients exhibiting symptoms of CMT2B or those with a family history of the condition, as it provides definitive genetic evidence of the RAB7A mutation. Early and accurate diagnosis through the RAB7A Gene CMT2B Genetic Test can significantly impact the management and treatment options for affected individuals, allowing for personalized care plans that can improve quality of life.
The test is available at DNA Labs UAE, a leading facility in genetic testing and diagnostics, ensuring high standards of accuracy and reliability. The cost of the test is set at 4400 AED, reflecting the specialized nature of the analysis and the sophisticated technology used to identify the genetic mutation. By opting for this test at DNA Labs UAE, patients and their families can expect comprehensive support, from the initial consultation through to the interpretation of results and guidance on subsequent steps.
The LMNA Gene CMT2B1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the LMNA gene, which are associated with Charcot-Marie-Tooth disease type 2B1 (CMT2B1). This genetic condition is part of a group of disorders known as Charcot-Marie-Tooth (CMT) disease, characterized by peripheral neuropathy leading to muscle weakness and atrophy, primarily affecting the limbs. The LMNA gene plays a crucial role in encoding proteins essential for the structural integrity and function of the cell nucleus. Mutations in this gene can disrupt these processes, contributing to the development of CMT2B1.
The test is conducted using a blood sample, where DNA is extracted and analyzed for specific genetic alterations in the LMNA gene. It is a vital tool for individuals with a family history of CMT2B1, offering them crucial information regarding their genetic status and risk of developing the condition. Moreover, it aids in the early diagnosis and management of the disease, allowing for timely intervention and support.
The cost of the LMNA Gene CMT2B1 Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the comprehensive analysis required to detect the presence of genetic mutations associated with CMT2B1, providing individuals and their families with essential insights into their genetic health and guiding future healthcare decisions.
The MED25 Gene CMT2B2 Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, designed to identify mutations in the MED25 gene, which are associated with Charcot-Marie-Tooth disease type 2B2 (CMT2B2). CMT2B2 is a subtype of Charcot-Marie-Tooth disease, a group of 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 as the condition progresses. The test is crucial for individuals with a family history of CMT2B2 or those showing symptoms, as it provides definitive genetic evidence of the condition. This information is vital for planning appropriate management and treatment strategies. The test cost is set at 4400 AED and is conducted with precision and care by the experienced professionals at DNA Labs UAE, ensuring reliable results for patients and their families.
The TRPV4 Gene CMT2C Genetic Test is a specialized diagnostic assessment offered by DNA Labs UAE, designed to identify mutations in the TRPV4 gene, which are associated with Charcot-Marie-Tooth disease type 2C (CMT2C). CMT2C is a rare form of Charcot-Marie-Tooth disease, a neurological disorder that affects the peripheral nerves, leading to muscle weakness and sensory loss primarily in the arms and legs. The TRPV4 gene plays a crucial role in the development and function of peripheral nerves, and mutations in this gene can disrupt nerve function, leading to the symptoms of CMT2C.
The test is conducted through a blood sample or a buccal swab, which is then analyzed to detect any genetic anomalies in the TRPV4 gene. This genetic test is pivotal for individuals who have a family history of CMT2C or exhibit symptoms related to peripheral neuropathies, as it can provide a definitive diagnosis of CMT2C. Early diagnosis through the TRPV4 Gene CMT2C Genetic Test can aid in the management and treatment of the condition, potentially improving the quality of life for affected individuals.
DNA Labs UAE offers this comprehensive genetic test for a cost of 4400 AED. The test is performed with high accuracy and confidentiality, ensuring that patients receive reliable results along with the necessary support and information to understand their condition better.
The GARS1 Gene CMT2D Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect mutations in the GARS1 gene that are associated with Charcot-Marie-Tooth disease type 2D (CMT2D). This condition is a type of inherited neurological disorder that affects the peripheral nerves, leading to muscle weakness and sensory problems primarily in the limbs. The test plays a crucial role in the early identification and management of CMT2D, enabling healthcare professionals to devise personalized treatment plans for affected individuals.
Performed using a sample of the patient's blood, the test specifically looks for genetic alterations in the GARS1 gene, which encodes an enzyme essential for the proper functioning of peripheral nerves. Identifying mutations in this gene can confirm a diagnosis of CMT2D, distinguish it from other forms of Charcot-Marie-Tooth disease, and help in understanding the inheritance pattern within families.
The cost of the GARS1 Gene CMT2D Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the sophisticated genetic analysis required to detect the relevant mutations, providing crucial information for affected individuals and their families. DNA Labs UAE is equipped with state-of-the-art technology and staffed by experts in genetics, ensuring accurate and reliable test results.
The HSPB1 gene CMT2F genetic test is a specialized diagnostic tool aimed at identifying mutations in the HSPB1 gene, which are linked to Charcot-Marie-Tooth disease type 2F (CMT2F). Charcot-Marie-Tooth disease is a group of inherited disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems, predominantly in the feet and legs. CMT2F is a specific subtype characterized by late-onset and predominantly affects motor nerves, though sensory nerves can also be involved.
The test involves analyzing the patient's DNA, extracted from a blood sample, to look for specific genetic alterations in the HSPB1 gene that are known to cause CMT2F. Identifying these mutations can confirm a diagnosis of CMT2F, which is crucial for managing the disease, understanding its progression, and providing appropriate genetic counseling for affected families.
The test is offered by DNA Labs UAE, a leading facility in genetic testing and analysis in the United Arab Emirates. The cost of the HSPB1 gene CMT2F genetic test 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 HSPB1 gene. By opting for this test at DNA Labs UAE, patients and their families can expect reliable results, professional genetic counseling, and guidance on the next steps following a diagnosis.
The MPZ Gene CMT2I Genetic Test is a specialized diagnostic procedure designed to detect mutations in the MPZ gene, which are associated with Charcot-Marie-Tooth disease type 2I (CMT2I). Charcot-Marie-Tooth disease is a group of hereditary disorders that affect the peripheral nerves, leading to muscle weakness and sensory loss, primarily in the arms and legs. The MPZ gene encodes for myelin protein zero, a critical component of the myelin sheath that insulates nerve fibers. Mutations in this gene can disrupt nerve function and lead to the symptoms observed in CMT2I.
This genetic test is crucial for individuals who exhibit symptoms of peripheral neuropathy, have a family history of Charcot-Marie-Tooth disease, or for whom there is a clinical suspicion of CMT2I. Early and accurate diagnosis through the MPZ Gene CMT2I Genetic Test can guide treatment options, inform prognosis, and assist with family planning decisions.
The test is available at DNA Labs UAE, a leading provider of genetic testing services in the United Arab Emirates. DNA Labs UAE utilizes state-of-the-art technology to ensure accurate and reliable test results. The cost of the MPZ Gene CMT2I Genetic Test is 4400 AED. This investment can provide individuals and families with crucial information about their genetic health, enabling them to make informed medical and lifestyle decisions.
The MPZ Gene CMT2J Genetic Test is a specialized diagnostic procedure offered at DNA Labs UAE, aimed at detecting mutations in the MPZ gene, which are linked to Charcot-Marie-Tooth disease type 2J (CMT2J). CMT2J is a rare form of the Charcot-Marie-Tooth disease, a group of disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems, primarily in the feet and legs, and sometimes affecting the hands and arms.
The MPZ gene plays a crucial role in the functioning and maintenance of myelin, the protective sheath covering nerve fibers. Mutations in this gene can disrupt nerve signal transmission, leading to the symptoms associated with CMT2J. Early and accurate detection of these mutations can aid in the diagnosis, allowing for better management and understanding of the disease's progression.
The test is priced at 4400 AED and is conducted at DNA Labs UAE, a leading facility known for its state-of-the-art genetic testing services. The test involves collecting a DNA sample, typically through a blood draw or cheek swab, which is then analyzed for specific mutations in the MPZ gene. Results from this test can provide crucial information for affected individuals and their families, including the confirmation of a CMT2J diagnosis, insight into the disease's progression, and guidance for genetic counseling.
The GDAP1 Gene CMT2K Genetic Test is a specialized diagnostic procedure aimed at identifying mutations in the GDAP1 gene, which are known to cause Charcot-Marie-Tooth disease type 2K (CMT2K), a specific form of Charcot-Marie-Tooth disease. This condition is a hereditary neurological disorder that affects the peripheral nerves, leading to muscle weakness and sensory problems primarily in the limbs.
The test is conducted by collecting a DNA sample, usually through a blood draw or cheek swab, which is then analyzed in the laboratory for the presence of specific genetic alterations in the GDAP1 gene. These mutations disrupt the normal function of the peripheral nerves, resulting in the symptoms associated with CMT2K.
Offered at DNA Labs UAE, the GDAP1 Gene CMT2K Genetic Test is priced at 4400 AED. DNA Labs UAE is a leading facility in the region, equipped with state-of-the-art technology and staffed by genetics professionals to ensure accurate and reliable test results. This test is crucial for individuals with a family history of Charcot-Marie-Tooth disease or those exhibiting symptoms, as it can confirm a diagnosis of CMT2K, inform treatment strategies, and aid in understanding the risk of passing the condition on to future generations.
The HSPB8 Gene CMT2L Genetic Test is a specific diagnostic tool used to identify mutations in the HSPB8 gene, which are associated with Charcot-Marie-Tooth disease type 2L (CMT2L). Charcot-Marie-Tooth disease is a group of hereditary disorders that affect the peripheral nerves, leading to muscle weakness and sensory problems, primarily in the feet and legs, and sometimes in the hands and arms. CMT2L is a subtype of this condition characterized by its genetic origin—the mutation in the HSPB8 gene.
This test is critical for individuals who have a family history of Charcot-Marie-Tooth disease or exhibit symptoms consistent with the condition. Early and accurate diagnosis through the HSPB8 Gene CMT2L Genetic Test can facilitate timely intervention, potential treatment options, and genetic counseling for affected individuals and their families.
The test is available at DNA Labs UAE, a reputable facility known for its comprehensive genetic testing services. The cost of the HSPB8 Gene CMT2L Genetic Test is 4400 AED. The testing process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for the presence of mutations in the HSPB8 gene. Results from this test can provide valuable information for the management and understanding of Charcot-Marie-Tooth disease type 2L.
