Understanding the Symptoms of MED25 Gene CMT2B2 Genetic Test The MED25 gene is crucial in understanding the complexities of Charcot-Marie-Tooth disease type 2B2 (CMT2B2), a condition that affects the peripheral nerves. DNA Labs UAE offers a comprehensive genetic test for the MED25 gene, aiding in the diagnosis and understanding of CMT2B2. This article explores the […]
Dr Padmaja
Symptoms and Testing information for TRPV4 Gene CMT2C Genetic Test
In the realm of genetic testing and diagnostics, understanding the intricate details of specific genes and their mutations is crucial for the identification and management of various inherited conditions. One such gene that has garnered significant attention is the TRPV4 gene, associated with Charcot-Marie-Tooth disease type 2C (CMT2C). DNA Labs UAE is at the forefront […]
Symptoms and Testing information for GARS1 Gene CMT2D Genetic Test
Charcot-Marie-Tooth disease type 2D (CMT2D) is a genetic disorder that affects the peripheral nerves. It is one of the many subtypes of Charcot-Marie-Tooth disease, which is the most common inherited disorder of the peripheral nervous system. CMT2D is specifically linked to mutations in the GARS1 gene, which plays a crucial role in the development and […]
Symptoms and Testing information for HSPB1 Gene CMT2F Genetic Test
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide valuable insights into your genetic makeup. One of the critical tests provided by DNA Labs UAE is the HSPB1 Gene CMT2F Genetic Test. This test is crucial for individuals suspecting they may have Charcot-Marie-Tooth disease type […]
Symptoms and Testing information for MPZ Gene CMT2I Genetic Test
Charcot-Marie-Tooth disease (CMT) represents a group of inherited disorders that affect the peripheral nerves, which are located outside the brain and spinal cord. Among the various types of CMT, Type 2I, linked to the MPZ gene, stands out due to its unique genetic background and symptomatology. Understanding the symptoms of MPZ Gene CMT2I is crucial […]
Symptoms and Testing information for MPZ Gene CMT2J Genetic Test
In the realm of genetic diagnostics and personalized medicine, understanding the intricate dance of our genetic makeup has never been more critical. Among the myriad of genetic conditions that have come to the forefront of scientific exploration, Charcot-Marie-Tooth disease type 2J (CMT2J) represents a particularly challenging puzzle. This condition, rooted in variations within the MPZ […]
Symptoms and Testing information for GDAP1 Gene CMT2K Genetic Test
Understanding GDAP1 Gene CMT2K Genetic Test The GDAP1 gene plays a critical role in the development and function of peripheral nerves. Mutations in this gene are associated with Charcot-Marie-Tooth disease type 2K (CMT2K), a subtype of Charcot-Marie-Tooth disease (CMT), which is a group of inherited disorders that affect the peripheral nerves. These nerves carry signals […]
Symptoms and Testing information for HSPB8 Gene CMT2L Genetic Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a wide range of services designed to provide insights into various genetic conditions. One of the critical tests provided by DNA Labs UAE is focused on the HSPB8 gene, which is associated with Charcot-Marie-Tooth disease type 2L (CMT2L), a form of hereditary […]
Symptoms and Testing information for AARS1 Gene CMT2N Genetic Test
— Understanding the Symptoms of AARS1 Gene CMT2N Genetic Test Charcot-Marie-Tooth disease (CMT) represents a group of inherited disorders that affect the peripheral nerves, which are located outside the brain and spinal cord. Among the various types of CMT, type 2N (CMT2N) is particularly noteworthy because it is caused by mutations in the AARS1 gene. […]
Symptoms and Testing information for EGR2 Gene CMT4E Genetic Test
Understanding the Symptoms of EGR2 Gene CMT4E Genetic Test Charcot-Marie-Tooth disease (CMT) represents a group of inherited disorders that affect the peripheral nerves, which are located outside the brain and spinal cord. One specific subtype of this condition, known as CMT4E, is caused by mutations in the EGR2 gene. This particular form of the disease […]