Understanding the KCTD17 Gene and DYT26 Myoclonic Disorder The KCTD17 gene, implicated in the development of DYT26 myoclonic disorder, has been a subject of extensive research in the field of genetics. This condition, which falls under the umbrella of neurological disorders, is characterized by its primary symptom: myoclonus. Myoclonus refers to sudden, involuntary muscle jerks […]
Understanding the symptoms of genetic disorders is crucial for early diagnosis and management. One such condition that has garnered attention in the medical community is related to mutations in the GNAL gene, also known as DYT25 dystonia. Dystonia is a movement disorder that causes muscles to contract involuntarily, leading to repetitive movements or abnormal postures. […]
Symptoms of ANO3 Gene DYT24 Genetic Test Dystonia is a complex neurological condition characterized by involuntary muscle contractions, which can result in twisting and repetitive movements or abnormal postures. Among the various genetic factors contributing to dystonia, the ANO3 gene has been identified as a significant player, particularly associated with a form known as DYT24. […]
At DNA Labs UAE, we are committed to providing comprehensive genetic testing services to help individuals understand their genetic makeup and potential health risks. One such test we offer is the CACNA1B Gene DYT23 Genetic Test. This test is specifically designed to detect mutations in the CACNA1B gene, which have been linked to DYT23, a […]
— Understanding the Symptoms of HPCA Gene DYT2 Genetic Test Genetic testing has become a cornerstone in the diagnosis and understanding of various inherited disorders. Among these, the HPCA gene DYT2 genetic test is crucial for diagnosing a specific form of dystonia. Dystonia is a movement disorder that causes muscles to contract involuntarily, leading to […]
Understanding the nuances of genetic disorders is crucial for early diagnosis and effective management. One such condition that has gained attention in the medical community is related to the SLC2A1 gene, known as DYT18. The SLC2A1 gene plays a vital role in the human body, encoding for the glucose transporter type 1 (GLUT1). This protein […]
In the ever-evolving field of genetics, understanding the intricacies of our DNA can lead to significant breakthroughs in diagnosing and managing various health conditions. One such advancement is the identification and analysis of the PRKRA gene, linked to DYT16 dystonia, a rare but impactful movement disorder. DNA Labs UAE is at the forefront of this […]
Understanding the symptoms of the ATP1A3 gene mutation, associated with DYT12 genetic disorder, is crucial for early diagnosis and effective management of the condition. DNA Labs UAE offers a comprehensive genetic test for this mutation, providing valuable insights into this rare but impactful condition. The test, priced at 4400 AED, is a critical tool for […]
In the realm of genetic testing, understanding the nuances of our DNA can provide invaluable insights into our health, predispositions, and potential medical conditions. One particular area of interest is the DRD2 gene, also associated with the DYT11 movement disorder. DNA Labs UAE is at the forefront of offering comprehensive genetic testing services, including the […]
— The SGCE gene, also known as the epsilon-sarcoglycan gene, plays a crucial role in the normal functioning of the brain, particularly in the movement control regions. Mutations in this gene are associated with a condition known as Myoclonus-Dystonia (MD), which is classified under the broader category of dystonia, DYT11. Understanding the symptoms of SGCE […]
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.
