Understanding the COX6A1 Gene and CMTRID The COX6A1 gene plays a crucial role in the body’s cellular energy production. It encodes a component of the cytochrome c oxidase (COX) complex, which is integral to the mitochondrial respiratory chain. Mutations in this gene can lead to cytochrome c oxidase deficiency, manifesting in various clinical symptoms and […]
In the realm of genetic testing, the GJB1 Gene CMTX1 Genetic Test stands out as a pivotal diagnostic tool. This test specifically targets the GJB1 gene mutations responsible for Charcot-Marie-Tooth disease type X1 (CMTX1), a condition that significantly impacts the nervous system. Understanding the symptoms of CMTX1 is crucial for individuals who may be at […]
In the realm of medical genetics, the LRSAM1 gene plays a significant role, especially in relation to Charcot-Marie-Tooth disease type 2P (CMT2P). This condition, a variant of the broader Charcot-Marie-Tooth (CMT) disease, affects the peripheral nerves. The genetic testing for the LRSAM1 gene is crucial for diagnosing, understanding, and managing CMT2P. DNA Labs UAE offers […]
— 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 […]
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 […]
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 […]
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 […]
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 […]
Understanding the RAB7A Gene and CMT2B Genetic Testing Charcot-Marie-Tooth disease type 2B (CMT2B) is a rare, inherited neurological disorder characterized by the degeneration of peripheral nerves. This leads to muscle weakness and sensory loss, primarily in the feet and hands. The condition is linked to mutations in the RAB7A gene, which plays a critical role […]
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 […]
DNA Labs UAE is a leading provider of genomics services in the United Arab Emirates. Our comprehensive range of services includes DNA sequencing, gene expression analysis, and SNP genotyping. With state-of-the-art equipment and a dedicated team of scientists and technicians, we ensure high-quality, accurate, and reliable data.
