Cone-rod dystrophy type 12 is a severe genetic disorder that affects the eyes, leading to a progressive loss of vision. This condition is caused by mutations in the PROM1 gene, which plays a crucial role in the normal functioning of the photoreceptors in the retina. The photoreceptors are responsible for capturing light and converting it […]
Symptoms of RPGRIP1 Gene Cone-Rod Dystrophy Type 13 Genetic Test Cone-rod dystrophy type 13, caused by mutations in the RPGRIP1 gene, is a rare genetic disorder that primarily affects the eyes. This condition is characterized by the progressive loss of cone and rod photoreceptor cells, which are crucial for vision. Individuals with this condition often […]
Cone-rod dystrophy type 14, caused by mutations in the GUCA1A gene, is a rare genetic disorder that affects the eyes’ ability to function properly. It is characterized by the progressive loss of vision, starting with color vision deficits and night blindness, eventually leading to a significant reduction in central and peripheral vision. Understanding the symptoms […]
Cone-Rod Dystrophy Type 15, caused by mutations in the CDHR1 gene, is a genetic condition that affects the retina and leads to progressive vision loss. This condition is characterized by the degeneration of the cone and rod photoreceptor cells in the retina, which are crucial for sharp, detailed central vision and color vision, as well […]
Cone-Rod Dystrophy Type 17, linked to mutations in the CD3G gene, is a rare genetic disorder that affects the eyes, leading to progressive vision loss. This condition is characterized by the deterioration of the cone and rod photoreceptor cells in the retina. The cone cells are responsible for color vision and visual acuity, while the […]
Cone-Rod Dystrophy Type 2, caused by mutations in the CRX gene, is a rare genetic disorder that affects the retina, leading to progressive vision loss. Understanding the symptoms and undergoing genetic testing can provide critical insights for individuals and families affected by this condition. DNA Labs UAE offers a comprehensive CRX Gene Cone-Rod Dystrophy Type […]
Understanding the genetic underpinnings of various diseases has become a cornerstone of modern medicine, enabling the development of targeted treatments and early interventions. Among these genetic conditions, Cone-Rod Dystrophy Type 20, caused by mutations in the POC1B gene, has garnered attention for its impact on vision. DNA Labs UAE stands at the forefront of genetic […]
Cone-Rod Dystrophy Type 3, also known as Stargardt disease, is a progressive eye disorder that leads to vision loss. This condition is primarily caused by mutations in the ABCA4 gene. Understanding the symptoms and undergoing genetic testing can be crucial for early diagnosis and management. DNA Labs UAE offers a comprehensive ABCA4 Gene Cone-Rod Dystrophy […]
Genetic testing has become a cornerstone in the diagnosis and understanding of numerous inherited conditions, allowing for early detection and personalized treatment plans. Among these conditions is Cone-Rod Dystrophy Type 4, a rare genetic disorder that primarily affects the eyes. DNA Labs UAE is at the forefront of providing advanced genetic testing services, including the […]
In the realm of genetic testing and diagnosis, understanding the nuances of specific genes and their implications on health is crucial. The PAX6 gene, pivotal in eye development and function, has garnered attention for its role in various ocular conditions, including Coloboma of the optic nerve. DNA Labs UAE stands at the forefront of genetic […]
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.
