In the realm of medical diagnostics, the understanding and identification of genetic conditions have become paramount in providing targeted and effective treatments. One such condition that has garnered attention in the field of hematology is Myelodysplastic Syndrome (MDS) associated with the deletion of the long arm of chromosome 20, known as del(20q) MDS. This condition, […]
Leber’s Hereditary Optic Neuropathy (LHON) is a rare genetic disorder that primarily affects the eyes and vision. It is characterized by the sudden loss of central vision, which is crucial for tasks such as reading, driving, and recognizing faces. LHON is caused by mutations in the mitochondrial DNA, and it is therefore inherited in a […]
Understanding Thalassemia Beta Mutation Analysis Test Thalassemia is a genetic blood disorder characterized by the reduction in hemoglobin production, which leads to anemia. Among its types, Beta Thalassemia is particularly significant due to its varied severity and genetic transmission patterns. It is caused by mutations in the HBB gene on chromosome 11, affecting the beta-globin […]
In the UAE, the health and well-being of newborns are of paramount importance, and one of the most crucial steps taken by parents towards ensuring their child’s health is opting for a comprehensive newborn screening panel. DNA Labs UAE is at the forefront of providing these essential services, offering a comprehensive test that screens for […]
Spinocerebellar Ataxia (SCA) is a term used for a group of hereditary ataxias that are characterized by degenerative changes in the part of the brain related to the control of movement, and often in the spinal cord. Among these, SCA-14 is a type that results from mutations in the PRKCG gene. This particular type of […]
Spinocerebellar Ataxia (SCA) encompasses a group of genetic disorders characterized by progressive degeneration of the cerebellum, the part of the brain responsible for coordinating movement. Among the various types, SCA-11 is particularly noteworthy due to its genetic basis in mutations of the TTBK2 gene. This mutation leads to a variety of symptoms that can severely […]
Spinocerebellar Ataxia Type 5 (SCA-5) is a rare, inherited condition that affects the cerebellum, the part of the brain responsible for controlling movement. This condition is caused by mutations in the SPTBN2 gene, which plays a crucial role in the development and maintenance of the cerebellum. Individuals with SCA-5 experience a progressive loss of coordination […]
Spinocerebellar ataxia type 8 (SCA-8) is a genetic disorder characterized by progressive coordination problems and other neurological symptoms. It is caused by mutations in the ATXN8OS and ATXN8 genes. Understanding the symptoms of SCA-8 and the availability of genetic testing can be crucial for individuals and families affected by this condition. DNA Labs UAE offers […]
In the realm of genetic testing and molecular diagnostics, understanding the significance of specific gene mutations is crucial for both patients and healthcare providers. One such mutation that has garnered attention is the PIK3CA mutation. This genetic alteration is associated with various forms of cancer, including breast cancer, colorectal cancer, and others, making its detection […]
Leigh Syndrome, a severe neurological disorder, manifests through a complex spectrum of symptoms that can perplex both families and healthcare professionals. It is a condition that primarily affects the central nervous system, leading to progressive loss of mental and movement abilities. Recognizing the symptoms early can be crucial for management and treatment. DNA Labs UAE […]
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.
