MELAS syndrome, which stands for Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes, is a complex genetic condition that affects various systems of the body, particularly the nervous system and muscles. It is caused by mutations in mitochondrial DNA, specifically in the MT-TF gene. Understanding the symptoms of MELAS syndrome is crucial for early diagnosis and […]
At DNA Labs UAE, we are dedicated to providing comprehensive genetic testing services to help individuals and families understand their genetic makeup and potential health risks. One of the critical tests we offer is for the MT-TC Gene MELAS Syndrome. This condition, which stands for Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes, is a rare […]
McKusick-Kaufman syndrome (MKKS), also known as Kaufman-McKusick syndrome, is a rare genetic disorder that affects multiple systems of the body. This condition is inherited in an autosomal recessive pattern, meaning that an individual must receive a defective gene from each parent to be affected. The MKKS gene, which plays a crucial role in the development […]
Understanding the complexities of genetic disorders is crucial for early diagnosis and management. Among these, the FBN1 gene mutation leading to MASS syndrome represents a significant concern due to its varied symptoms and impact on multiple body systems. DNA Labs UAE stands at the forefront of genetic testing, offering comprehensive solutions including the FBN1 Gene […]
Marfan syndrome is a genetic disorder that affects the body’s connective tissue, which plays a crucial role in supporting and structuring the skin, blood vessels, eyes, heart, and other organs. The condition is primarily caused by mutations in the FBN1 gene, which encodes a protein essential for the formation of elastic fibers found in connective […]
Long QT syndrome (LQTS) is a disorder of the heart’s electrical activity that can cause sudden, uncontrollable, and dangerous arrhythmias. Type 9 Long QT syndrome, specifically linked to mutations in the CAV3 gene, is a rare form of this condition. DNA Labs UAE offers a comprehensive genetic test for those concerned about the potential risks […]
In the realm of genetic testing, the advancement in identifying specific genetic disorders has been monumental. Among these, the CACNA1C gene test for Long QT Syndrome type 8 (LQTS8) is particularly significant. This genetic condition, while rare, can have profound implications on an individual’s health, making awareness and early detection crucial. DNA Labs UAE stands […]
Long QT Syndrome (LQTS) is a disorder of the heart’s electrical activity. It can cause sudden, uncontrollable, dangerous arrhythmias (abnormal heart rhythms) in response to exercise or stress. These arrhythmias can be life-threatening, leading to fainting, seizures, or even sudden death. Among the various types, Long QT Syndrome Type 6 is caused by mutations in […]
Long QT Syndrome (LQTS) is a rare, inherited heart condition that can lead to serious or even life-threatening arrhythmias. Among the genetic variants that can cause LQTS, mutations in the KCNE1 gene are responsible for Long QT Syndrome Type 5 (LQT5). Understanding the symptoms and getting an accurate diagnosis is crucial for managing the condition […]
Long QT syndrome (LQTS) is a rare heart condition that can potentially lead to life-threatening arrhythmias. Among the various types of LQTS, type 4, also known as Andersen-Tawil syndrome, is associated with mutations in the ANK2 gene. DNA Labs UAE offers a comprehensive genetic test for this condition, aimed at individuals who exhibit symptoms or […]
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.
