Spinocerebellar ataxia type 26 (SCA26), linked to the EEF2 gene, represents a rare, autosomal dominant neurological disorder characterized by progressive ataxia – a condition marked by coordination problems due to cerebellar dysfunction. This disorder underscores the importance of genetic testing for early diagnosis and management. DNA Labs UAE offers a comprehensive genetic test for SCA26, […]
In the realm of genetic disorders, Spinocerebellar Ataxia Type 11 (SCA11) holds a significant yet challenging position. This condition, caused by mutations in the TTBK2 gene, is inherited in an autosomal dominant pattern. Understanding its symptoms and the importance of genetic testing can be pivotal for affected individuals and their families. DNA Labs UAE offers […]
Spinocerebellar ataxia type 27 (SCA27) is a challenging and progressive neurological disorder that falls under the umbrella of genetic conditions known as spinocerebellar ataxias. This particular form, SCA27, is caused by mutations in the FGF14 gene and is inherited in an autosomal dominant manner, meaning a single copy of the altered gene in each cell […]
In the realm of genetic testing, advancements have paved the way for the identification and understanding of numerous genetic disorders that were once shrouded in mystery. Among these, Spinocerebellar Ataxia Type 12 (SCA12), caused by mutations in the PPP2R2B gene, stands out due to its unique symptoms and inheritance pattern. DNA Labs UAE is at […]
In the realm of genetic testing, understanding the nuances of specific genes and their associated conditions is paramount for both patients and healthcare professionals. One such gene, the AFG3L2 gene, is linked to Spinocerebellar Ataxia Type 28 (SCA28), a condition that falls under the category of autosomal dominant genetic disorders. This article aims to shed […]
Spinocerebellar ataxia type 12 (SCA12) is a rare, genetic disorder characterized by progressive loss of motor control and coordination. This condition is caused by mutations in the WWOX gene, which plays a critical role in the development and function of the nervous system. Understanding the symptoms of WWOX gene spinocerebellar ataxia type 12 and the […]
DNA Labs UAE is at the forefront of genetic testing and analysis, offering a comprehensive range of services designed to provide individuals with insights into their genetic makeup. Among the various tests available, the KCNC3 Gene Spinocerebellar Ataxia Type 13 Autosomal Dominant Genetic Test is a critical tool for individuals and families concerned about the […]
Understanding Spinocerebellar Ataxia Type 13 (SCA13) Linked to the GRM1 Gene Spinocerebellar ataxia type 13 (SCA13) is a rare, autosomal recessive neurological disorder characterized by a wide range of symptoms, primarily affecting the cerebellum – the part of the brain that controls coordination and balance. This disorder is caused by mutations in the GRM1 gene, […]
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 […]
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.
