Symptoms of UNC119 Gene Cone-Rod Dystrophy Genetic Test Cone-rod dystrophy is a group of inherited eye disorders that affect the light-sensitive cells of the retina. The UNC119 gene plays a significant role in the development and function of these cells. Mutations in the UNC119 gene can lead to a form of cone-rod dystrophy, where the […]
At DNA Labs UAE, we understand the importance of accurate genetic testing for the diagnosis and management of various genetic conditions. One such condition that affects the eyes is Cone-Rod Dystrophy Type 11, caused by mutations in the RAX2 gene. This rare disorder can significantly impact an individual’s vision, making early detection and intervention crucial. […]
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 […]
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.
