— Understanding the symptoms of a genetic condition is crucial for early diagnosis and management. One such condition, related to the CTDP1 gene, is a form of Charcot-Marie-Tooth disease known as CMT4. This article delves into the symptoms associated with this condition and introduces the CTDP1 Gene CMT4 CTDP1 Related Genetic Test available at DNA […]
Dr Padmaja
Symptoms and Testing information for GDAP1 Gene CMT4A Genetic Test
Understanding the nuances of genetic conditions is crucial for early diagnosis and management. Among these, Charcot-Marie-Tooth disease type 4A (CMT4A) stands out due to its genetic basis and the significant impact it can have on an individual’s quality of life. The GDAP1 gene plays a pivotal role in this condition, and identifying mutations within this […]
Symptoms and Testing information for MTMR2 Gene CMT4B1 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 4B1, caused by mutations in the MTMR2 gene, is particularly noteworthy for its distinct clinical features and inheritance patterns. Recognizing the symptoms associated with this […]
Symptoms and Testing information for SBF2 Gene CMT4B2 Genetic Test
In the realm of genetic testing and diagnostics, understanding the nuances of specific genetic conditions is paramount for both healthcare professionals and patients. One such condition that has garnered attention is Charcot-Marie-Tooth disease type 4B2 (CMT4B2), caused by mutations in the SBF2 gene. DNA Labs UAE is at the forefront of providing comprehensive genetic testing […]
Symptoms and Testing information for SH3TC2 Gene CMT4C Genetic Test
In the realm of genetic diagnostics, DNA Labs UAE stands at the forefront, offering a comprehensive range of tests designed to unlock the mysteries of our genetic makeup. Among the myriad of tests available, the SH3TC2 Gene CMT4C Genetic Test is of paramount importance for individuals showing symptoms or having a family history of Charcot-Marie-Tooth […]
Symptoms and Testing information for NDRG1 Gene CMT4D Genetic Test
Charcot-Marie-Tooth disease type 4D (CMT4D), also known as hereditary motor and sensory neuropathy Lom type, is a rare genetic disorder that affects the peripheral nerves. It is caused by mutations in the NDRG1 gene. This condition is part of a group of disorders known as Charcot-Marie-Tooth diseases, which are characterized by nerve degeneration and varying […]
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 […]
Symptoms and Testing information for MPZ 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. Among the various types of CMT, Type 4E, also known as CMT4E, is caused by mutations in the MPZ gene. Understanding the symptoms of this condition is crucial for early diagnosis and […]
Symptoms and Testing information for PMP22 Gene CMT1E Genetic Test
Charcot-Marie-Tooth disease (CMT) represents one of the most common inherited neurological disorders, affecting approximately 1 in 2,500 people worldwide. Among the various types of CMT, Type 1E (CMT1E), associated with mutations in the PMP22 gene, is particularly noteworthy due to its unique clinical manifestations and inheritance patterns. Understanding the symptoms of CMT1E is crucial for […]
Symptoms and Testing information for KIF1B Gene CMT2A1 Genetic Test
Charcot-Marie-Tooth disease (CMT) represents one of the most common hereditary neurological disorders, affecting the peripheral nerves. Among its various subtypes, CMT2A1, caused by mutations in the KIF1B gene, stands out due to its distinct clinical manifestations and inheritance patterns. Understanding the symptoms and opting for a genetic test can be a critical step in managing […]