Neutral Lipid Storage Disease with Myopathy (NLSDM) is a rare genetic disorder characterized by the abnormal accumulation of neutral lipids in various tissues of the body, including muscle tissue. This condition is primarily caused by mutations in the PNPLA2 gene, which plays a crucial role in the breakdown of triglycerides in the body. Identifying the […]
Understanding the symptoms of CCT5 Gene Neuropathy Hereditary Sensory with Spastic Paraplegia is crucial for early diagnosis and management of this condition. This genetic disorder, which affects the peripheral nervous system, can lead to a range of symptoms that significantly impact the quality of life of those affected. DNA Labs UAE offers a comprehensive genetic […]
Understanding the complexities of genetic conditions is a pivotal aspect of modern healthcare. Among these, the ATL3 gene neuropathy, also known as Hereditary Sensory Neuropathy Type 1F (HSN1F), is a condition that has garnered significant attention. This particular neuropathy is a genetic disorder that affects the peripheral nervous system, leading to a range of sensory […]
Understanding the nuances of genetic conditions is pivotal in the realm of medical science, especially when it comes to neuropathies that affect the sensory functions of the human body. One such condition is the Hereditary Sensory Neuropathy Type 1D (HSN1D), a rare disorder that significantly impacts the sensory nerves. It is primarily caused by mutations […]
Understanding the complexities of genetic disorders is pivotal in modern medicine, especially when dealing with conditions as nuanced and rare as DST Gene Neuropathy Hereditary Sensory and Autonomic Type 6 (HSAN6). This condition, although not widely known, has profound implications for those affected and their families. DNA Labs UAE stands at the forefront of genetic […]
Understanding the complexities of genetic conditions is crucial for early diagnosis and appropriate management. One such condition that has garnered attention in the medical community is SCN9A Gene Neuropathy, also known as Hereditary Sensory and Autonomic Neuropathy Type 2 (HSAN2). This rare genetic disorder is characterized by a variety of symptoms that can significantly impact […]
Understanding the symptoms of SPTLC2 Gene Neuropathy Hereditary Sensory and Autonomic Type 1C is crucial for early diagnosis and management of this rare genetic condition. At DNA Labs UAE, we offer a comprehensive genetic test for this condition, providing insights and guidance for affected individuals and their families. This test is priced at 4400 AED, […]
Genetic testing has become a cornerstone in diagnosing and understanding various hereditary conditions. Among these, neuropathies, which are disorders affecting the peripheral nerves, represent a significant category. One such condition is caused by mutations in the BSCL2 gene, leading to a specific type of neuropathy known as Distal Hereditary Motor Type 5A. DNA Labs UAE […]
Understanding the complexities of genetic conditions is crucial for early diagnosis and treatment. One such condition that has garnered attention in the medical community is POLG gene neuropathy with sensory ataxic dysarthria and ophthalmoparesis. This genetic disorder, although rare, presents a spectrum of symptoms that can significantly impact an individual’s quality of life. In response […]
Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) is a genetic disorder that affects the peripheral nerves, which are responsible for sending signals between the brain and the muscles, as well as sensory information back to the brain. This condition is caused by mutations in the PMP22 gene, which plays a crucial role in the […]
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.
