At DNA Labs UAE, we understand the importance of accurate and timely genetic testing for various conditions, including Doyne honeycomb retinal dystrophy (DHRD), a rare, inherited eye disorder. Our EFEMP1 gene test is designed to detect mutations in the EFEMP1 gene, which are responsible for DHRD. This detailed article aims to shed light on the […]
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Symptoms and Testing information for PXDN Gene Corneal opacification and other ocular anomalies Genetic Test
Symptoms of PXDN Gene Corneal Opacification and Other Ocular Anomalies Corneal opacification and other ocular anomalies associated with the PXDN gene present a complex challenge for individuals affected by this genetic condition. The PXDN gene plays a crucial role in eye development and its mutations can lead to a variety of ocular symptoms. Understanding these […]
Symptoms and Testing information for NLRP1 Gene Corneal intraepithelial dyskeratosis and ectodermal dysplasia Genetic Test
Symptoms of NLRP1 Gene Corneal Intraepithelial Dyskeratosis and Ectodermal Dysplasia Understanding the symptoms of NLRP1 gene corneal intraepithelial dyskeratosis and ectodermal dysplasia is crucial for early diagnosis and treatment. This genetic condition, although rare, affects multiple body systems, including the skin, hair, teeth, and eyes. Individuals with mutations in the NLRP1 gene often exhibit a […]
Symptoms and Testing information for SLC4A11 Gene Corneal endothelial dystrophy type 2 Genetic Test
DNA Labs UAE is at the forefront of genetic diagnostics, offering a comprehensive array of tests aimed at deciphering the complex code embedded within our DNA. Among these, the SLC4A11 Gene Corneal Endothelial Dystrophy Type 2 Genetic Test stands out for its crucial role in diagnosing a rare but impactful eye disorder. This test, priced […]
Symptoms and Testing information for VSX1 Gene Corneal dystrophy posterior polymorphous type 1 Genetic Test
Corneal dystrophies are a group of genetic eye disorders that primarily affect the cornea, the clear outer layer of the eye. Among these, Posterior Polymorphous Corneal Dystrophy type 1 (PPCD1) is a rare condition that can lead to vision impairment and, in severe cases, loss of vision. It is primarily associated with mutations in the […]
Symptoms and Testing information for TGFBI Gene Corneal dystrophy epithelial basement membrane Genetic Test
In the realm of genetic diagnostics, the identification of specific gene mutations that contribute to hereditary diseases is a crucial step in providing personalized medicine and targeted treatments. Among these genetic conditions, corneal dystrophies, particularly those associated with the TGFBI gene, have garnered significant attention due to their impact on vision and quality of life. […]
Symptoms and Testing information for CACNA1F Gene Cone-rod dystrophy X-linked type 3 Genetic Test
Cone-rod dystrophy X-linked type 3, associated with mutations in the CACNA1F gene, is a rare genetic disorder that affects the retina. This condition leads to the progressive loss of vision due to the degeneration of cone and rod photoreceptor cells in the eye. Understanding the symptoms and the availability of genetic testing is crucial for […]
Symptoms and Testing information for C21orf2 Gene Cone-rod dystrophy C21orf2 related Genetic Test
Cone-rod dystrophy is a group of inherited eye disorders that affect the retina. One of the genetic causes of this condition has been identified as mutations in the C21orf2 gene. Understanding the symptoms and seeking early diagnosis through genetic testing can significantly impact the management and quality of life of individuals affected by this condition. […]
Symptoms and Testing information for ADAM9 Gene Cone-Rod Dystrophy Type 9 Genetic Test
Cone-rod dystrophies (CRDs) are a group of inherited eye disorders that affect the cone cells and rod cells in the retina. These cells are crucial for vision, with cones providing color vision and sharp central vision, and rods enabling peripheral and night vision. One specific form of this condition, associated with mutations in the ADAM9 […]
Symptoms and Testing information for RIMS1 Gene Cone-Rod Dystrophy Type 7 Genetic Test
DNA Labs UAE is at the forefront of genetic testing and diagnostics, offering a comprehensive suite of tests designed to provide critical insights into your genetic makeup and potential health risks. Among the various tests available, the RIMS1 Gene Cone-Rod Dystrophy Type 7 Genetic Test is particularly significant for individuals experiencing symptoms related to vision […]