— 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. […]
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 […]
DNA Labs UAE is at the forefront of genetic testing and diagnosis, offering a wide range of services designed to provide insights into various genetic conditions. Among these is the specialized genetic test for VLDLR Gene Cerebellar Hypoplasia and Mental Retardation with or without Quadrupedal Locomotion Type 1, a rare genetic disorder that affects brain […]
In the realm of genetic testing and diagnostics, understanding the nuances of specific genetic conditions is paramount for both medical professionals and patients. One such condition, linked to the EGR2 gene, is Charcot-Marie-Tooth disease type 1D (CMT1D), a neurological disorder that affects the peripheral nerves. DNA Labs UAE is at the forefront of providing comprehensive […]
Cerebral Amyloid Angiopathy (CAA) is a neurological condition characterized by the accumulation of amyloid proteins in the walls of the arteries in the brain. This accumulation can lead to a range of symptoms and complications, including hemorrhagic stroke. One of the genes associated with an increased risk of developing CAA is the CST3 gene. Recognizing […]
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 […]
Cerebral Amyloid Angiopathy (CAA) is a neurological condition characterized by the accumulation of amyloid proteins in the walls of the arteries in the brain. This accumulation can lead to a variety of symptoms and is closely associated with the APP gene. DNA Labs UAE offers a comprehensive genetic test for those concerned about their risk […]
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 […]
In the realm of medical science, understanding the genetic predispositions to certain conditions is a critical step in preventative healthcare. One such condition, cerebral infarction, commonly known as a stroke, has been linked to various genetic factors, including mutations in the PRKCH gene. DNA Labs UAE stands at the forefront of genetic testing, offering a […]
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 2A2, caused by mutations in the MFN2 gene, is particularly noteworthy. Recognizing the symptoms of this condition is crucial for early diagnosis and management. At […]
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.
