Symptoms of CRYAB Gene Cataract Posterior Polar Type 2 Genetic Test The CRYAB gene, known for its critical role in encoding the alpha-crystallin B chain, is integral to the clarity and function of the human lens. Mutations in the CRYAB gene are directly linked to the development of Cataract Posterior Polar Type 2, a condition […]
Dr Padmaja
Symptoms and Testing information for MAF Gene Cataract Pulverulent or Cerulean with or without Microcornea Genetic Test
Understanding the complexities of genetic disorders is essential in today’s medical landscape, especially when it comes to conditions that can significantly impact quality of life from a very young age. One such condition involves the mutation of the MAF gene, which has been linked to specific types of cataracts, namely Pulverulent and Cerulean cataracts, with […]
Symptoms and Testing information for NHS Gene Cataract X-Linked Genetic Test
Understanding the genetic underpinnings of various health conditions is a cornerstone of modern medical science. Among these conditions, cataracts represent a significant area of concern due to their potential to impair vision severely. Particularly, the NHS gene cataract, which is linked to the X chromosome, has garnered attention for its unique genetic transmission patterns and […]
Symptoms and Testing information for GJA8 Gene Cataract-Microcornea Syndrome Genetic Test
DNA Labs UAE is at the forefront of genetic testing, offering a wide range of services to help individuals understand their genetic makeup and its implications on their health. Among these, the GJA8 Gene Cataract-Microcornea Syndrome Genetic Test stands out for its crucial role in diagnosing a rare but significant condition that affects the eyes. […]
Symptoms and Testing information for IARS2 Gene Cataracts Growth Hormone Deficiency Genetic Test
Understanding the intricate relationship between genetics and health is a journey that has fascinated scientists and medical professionals for decades. The IARS2 gene is a significant focus of this exploration, especially due to its association with a unique combination of symptoms that include cataracts, growth hormone deficiency, and more. DNA Labs UAE is at the […]
Symptoms and Testing information for ACO2 Gene Cerebellar-Retinal Degeneration Infantile Genetic Test
In recent years, the understanding of genetic conditions has significantly advanced, allowing for the early detection and management of various inherited diseases. One such condition is the ACO2 gene-related cerebellar-retinal degeneration, a rare infantile genetic disorder that can have severe impacts on affected individuals. DNA Labs UAE is at the forefront of providing comprehensive genetic […]
Symptoms and Testing information for PRPH2 Gene Choroidal Dystrophy Central Areolar Type 2 Genetic Test
At DNA Labs UAE, we understand the importance of genetic testing in diagnosing and managing genetic disorders. One such condition that can significantly affect individuals is Choroidal Dystrophy Central Areolar Type 2, a rare eye disorder that can lead to vision loss. This condition is associated with mutations in the PRPH2 gene. Our state-of-the-art laboratory […]
Symptoms and Testing information for CTC1 Gene Coat Plus Syndrome Genetic Test
DNA Labs UAE is at the forefront of genetic testing and analysis, offering a wide array of services designed to provide insights into one’s genetic makeup. Among these services is the CTC1 Gene Coat Plus Syndrome Genetic Test, a comprehensive examination aimed at detecting the presence of mutations in the CTC1 gene, which can indicate […]
Symptoms and Testing information for RGS9 Gene Bradyopsia Genetic Test
Symptoms of RGS9 Gene Bradyopsia Genetic Test Bradyopsia, a rare genetic condition, significantly impacts the lives of those affected by it. This condition, rooted in mutations within the RGS9 gene, disrupts the normal function of the retina. Individuals with bradyopsia experience a delayed adaptation of their vision to changes in light intensity, which can profoundly […]
Symptoms and Testing information for RGS9BP Gene Bradyopsia Genetic Test
Understanding Bradyopsia and the Role of RGS9BP Gene Bradyopsia, a rare genetic condition, profoundly affects the way individuals perceive motion. This condition, characterized by a delayed adaptation of the eyes to changes in light intensity, can significantly impact the quality of life, making everyday tasks challenging. At the heart of this condition lies the RGS9BP […]