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 10 (SCA10) is a progressive neurodegenerative disorder characterized by a wide array of symptoms. It is caused by mutations in the ATXN10 gene, which is inherited in an autosomal dominant pattern. This means that an individual only needs a single copy of the mutated gene from one parent to be affected by […]
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 10 (SCA10) is a rare genetic disorder that affects the central nervous system, leading to a progressive loss of muscle coordination and balance. This condition is caused by mutations in the ANO10 gene and is inherited in an autosomal recessive pattern. Understanding the symptoms and genetic basis of SCA10 is crucial for […]
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 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.
