Understanding PRKCG Gene Spinocerebellar Ataxia Type 14 Spinocerebellar ataxia type 14 (SCA14) is a progressive neurodegenerative disorder characterized by a wide array of symptoms, primarily affecting motor coordination. This condition is caused by mutations in the PRKCG gene, which plays a crucial role in the functioning of neurons in the cerebellum. The cerebellum is the […]
Spinocerebellar ataxia type 15 (SCA15) is a genetic disorder characterized by progressive ataxia, which is a condition marked by coordination problems and unsteady movements. This condition is caused by mutations in the ITPR1 gene, which plays a critical role in the functioning of nerve cells in the brain. Understanding the symptoms and undergoing genetic testing […]
Symptoms of DNAJB2 Gene Spinal Muscular Atrophy Type 5 Spinal Muscular Atrophy Type 5, caused by mutations in the DNAJB2 gene, is a rare genetic disorder that affects the motor neurons, leading to muscle weakness and atrophy. This condition is part of a group of hereditary diseases that impair the control of muscle movement. Understanding […]
Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy (SMA-PME) is a rare, genetic disorder characterized by progressive muscle weakness and wasting (atrophy), along with an uncontrolled jerking movement known as myoclonic epilepsy. This condition is caused by mutations in the ASAH1 gene, which plays a crucial role in the metabolism of certain fats in the body. […]
— Spinal Muscular Atrophy Distal X-Linked, associated with mutations in the ATP7A gene, is a rare genetic disorder that can have profound implications on the health and development of affected individuals. DNA Labs UAE offers a comprehensive genetic test for this condition, helping families and individuals gain crucial insights into their genetic health. Understanding the […]
Understanding the symptoms of a genetic condition is crucial for early diagnosis and management. One such condition that has garnered attention in the medical community is related to the FLRT1 gene, known as SPG68. This article delves into the symptoms associated with the FLRT1 gene mutation, the importance of the FLRT1 Related Genetic Test, and […]
Spinal Muscular Atrophy Lower Extremity Autosomal Dominant Type 2 (SMA-LED2) is a rare genetic disorder characterized by muscle weakness and atrophy, predominantly affecting the lower limbs. It is caused by mutations in the BICD2 gene. Understanding the symptoms of this condition is crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic […]
Symptoms of SPG7 Gene Mutation SPG7, also known as Spastic Paraplegia 7, is a genetic condition that primarily affects the legs and lower body, leading to progressive weakness and spasticity. This condition is a result of mutations in the SPG7 gene, which plays a crucial role in the maintenance and function of mitochondria, the energy-producing […]
Sure, here’s the article structured as per your instructions: Understanding the DYNC1H1 Gene and Its Impact on Spinal Muscular Atrophy Spinal Muscular Atrophy (SMA) is a genetic disorder that affects the control of muscle movement. It is caused by a loss of specialized nerve cells, called motor neurons, in the spinal cord and the part […]
— The ZFR gene, also known as Zinc Finger RNA binding protein, plays a crucial role in our genetic makeup, and mutations in this gene can lead to various health issues. One of the conditions associated with mutations in the ZFR gene is Spastic Paraplegia 71 (SPG71), a form of hereditary spastic paraplegia. This condition […]
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.
