Spinocerebellar ataxia type 31 (SCA31) is a neurodegenerative disorder characterized by progressive ataxia, which affects coordination and balance. This condition is part of a group of genetic disorders known as autosomal dominant cerebellar ataxias, which are caused by degeneration of the cerebellum and its associated pathways. Among the genes associated with this condition, the BEAN1 […]
Spinocerebellar Ataxia Type 3 (SCA3), also known as Machado-Joseph Disease, is a progressive neurodegenerative disorder that affects the cerebellum—the part of the brain that controls muscle movement. This condition is caused by a genetic mutation in the ATXN3 gene and is inherited in an autosomal dominant pattern. This means that only one copy of the […]
Spinocerebellar ataxia type 29 (SCA29) is a rare genetic disorder that is congenital and nonprogressive. It is characterized by early-onset cerebellar ataxia, which affects coordination and balance. This condition is caused by mutations in the ITPR1 gene, which plays a crucial role in the signaling pathways within cells, particularly in the cerebellum, which is the […]
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 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 […]
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, […]
DNA Labs UAE is at the forefront of genetic testing, offering a comprehensive range of services designed to provide insights into your genetic makeup and potential health risks. Among the tests offered is the PDYN Gene Spinocerebellar Ataxia Type 23 Autosomal Dominant Genetic Test. This test is crucial for individuals who have a family history […]
Spinocerebellar ataxia type 22 (SCA22) is a neurological disorder characterized by a wide array of symptoms, primarily affecting coordination and movement. This condition is caused by mutations in the KCND3 gene and is inherited in an autosomal dominant manner, meaning that only one copy of the altered gene is sufficient to cause the disorder. DNA […]
Spinocerebellar ataxia type 21 (SCA21) is a rare, inherited neurological disorder characterized by progressive problems with movement. This condition is caused by mutations in the TMEM240 gene, which plays a critical role in the functioning of the cerebellum, the part of the brain that controls coordination and balance. Understanding the symptoms of this condition is […]
In the realm of genetic testing and diagnosis, advancements have significantly improved our understanding of hereditary diseases. One such condition that has gained attention due to its impact on motor control and coordination is Spinocerebellar Ataxia Type 2 (SCA2), a disorder linked to the ATXN2 gene. This condition is autosomal dominant, meaning that only one […]
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.
