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 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 […]
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 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 […]
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. […]
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 […]
Symptoms of AIPL1 Gene Cone-Rod Dystrophy Genetic Test AIPL1 gene cone-rod dystrophy is a rare genetic disorder that affects the retina, leading to progressive vision loss. This condition is caused by mutations in the AIPL1 gene, which plays a crucial role in the health and function of photoreceptor cells in the retina. These cells are […]
At DNA Labs UAE, we are committed to providing our clients with comprehensive genetic testing services, including the TENM1 Gene Colobomatous Microphthalmia Genetic Test. This particular test is crucial for individuals who are at risk of or are showing symptoms of colobomatous microphthalmia, a rare genetic condition that can significantly impact ocular health. Understanding Colobomatous […]
Understanding YAP1 Gene Coloboma Ocular with or without Hearing Impairment, Cleft Lip/Palate, and/or Mental Retardation The YAP1 gene plays a crucial role in human development, influencing various physical and cognitive aspects. Mutations in this gene can lead to a complex spectrum of conditions, which may include ocular coloboma, hearing impairment, cleft lip and/or palate, and […]
Coloboma is a rare condition that affects the normal structure of the eye, leading to potential vision impairment. It can occur in one or both eyes and might affect various parts of the eye, including the iris, lens, retina, and optic nerve. This condition is often associated with the PAX6 gene, which plays a significant […]
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.
