Alternating hemiplegia of childhood (AHC) type 2 is a rare neurological disorder that can significantly impact the lives of those affected and their families. This condition is primarily caused by mutations in the ATP1A3 gene. Understanding the symptoms and undergoing genetic testing can be crucial for diagnosis and management. DNA Labs UAE offers a comprehensive […]
Glaucoma is a group of eye conditions that can lead to vision loss and blindness by damaging the optic nerve, which is vital for good vision. One specific form of glaucoma, Open Angle Glaucoma, has a genetic component that can be identified through genetic testing. In particular, mutations in the WDR36 gene have been associated […]
Glaucoma is a group of eye conditions that can lead to vision loss by damaging the optic nerve, often associated with increased pressure in the eye. Primary Congenital Glaucoma (PCG) is a severe form of glaucoma that appears early in life, ranging from birth to the first few years. Among the genetic variations contributing to […]
Glaucoma is a group of eye conditions that damage the optic nerve, the health of which is crucial for good vision. This damage is often caused by an abnormally high pressure in your eye and can lead to blindness if not treated. Among the various types of glaucoma, Primary Congenital Glaucoma (PCG) is a rare, […]
Gyrate atrophy of the choroid and retina is a rare, inherited condition that can lead to progressive vision loss. This condition is caused by mutations in the OAT gene, which lead to a deficiency of the enzyme ornithine aminotransferase. This enzyme plays a crucial role in the metabolism of amino acids in the body. When […]
In the realm of genetic diagnostics and disease prevention, understanding the implications of specific gene mutations is paramount. Among these, the RB1 gene plays a critical role, particularly in the context of hereditary retinoblastoma. DNA Labs UAE stands at the forefront of genetic testing, offering comprehensive insights into the RB1 gene’s mutations through the RB1 […]
Hermansky-Pudlak Syndrome (HPS) is a rare genetic disorder that affects multiple organs of the body. Among its various types, Type 4, caused by mutations in the HPS4 gene, presents unique challenges and symptoms for those affected. Understanding these symptoms and the availability of genetic testing for HPS4 can empower individuals and families to manage the […]
Hermansky-Pudlak Syndrome (HPS) is a rare genetic disorder that can significantly impact an individual’s health and quality of life. Among the various types of this syndrome, Type 1, associated with mutations in the HPS1 gene, is particularly notable for its symptoms and health implications. DNA Labs UAE offers a comprehensive genetic test for this condition, […]
Hermansky-Pudlak Syndrome (HPS) is a rare genetic disorder that affects multiple organs of the body. It is characterized by a lack of pigmentation (albinism), bleeding disorders, and lung and bowel diseases. Among its types, Hermansky-Pudlak Syndrome type 2 (HPS-2) is caused by mutations in the AP3B1 gene. This particular type not only shares common symptoms […]
Understanding Hermansky-Pudlak Syndrome Type 3 (HPS3) Hermansky-Pudlak Syndrome (HPS) is a rare genetic disorder that affects multiple organs of the body. Among its various types, Type 3, caused by mutations in the HPS3 gene, is significant for its clinical manifestations. It is characterized by a triad of symptoms: oculocutaneous albinism (a condition affecting the coloring […]
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.
