— Ectopia lentis is a condition characterized by the displacement or malposition of the crystalline lens of the eye. This condition can occur due to various reasons, but when it is specifically linked to a genetic cause, the FBN1 gene is often involved. The FBN1 gene is responsible for the production of fibrillin-1, a protein […]

Ectopia lentis et pupillae is a rare genetic disorder characterized by the dislocation of the lens and pupil of the eye. This condition is primarily caused by mutations in the ADAMTSL4 gene. Understanding the symptoms associated with this condition is crucial for early diagnosis and treatment. DNA Labs UAE offers a comprehensive genetic test for […]

Glaucoma is a group of eye conditions that can cause blindness by damaging the optic nerve, which is vital for good vision. This damage is often caused by an abnormally high pressure in your eye. One of the genetic factors associated with the development of early-onset glaucoma is the COL15A1 gene. Understanding the role of […]

Symptoms of ADAR Gene Dyschromatosis Symmetrica Hereditaria Dyschromatosis symmetrica hereditaria (DSH) is a rare genetic disorder, primarily affecting the skin. It is characterized by a mixture of hyperpigmented and hypopigmented macules, mainly on the backs of the hands and feet, and sometimes on the face. These skin changes typically appear in infancy or early childhood […]

Duane Retraction Syndrome (DRS) is a congenital eye movement disorder that restricts the eye’s ability to move outward toward the ear (abduction) and, in some cases, to move inward toward the nose (adduction). This condition, which can affect one or both eyes, is often diagnosed in early childhood. Among the genes associated with DRS, mutations […]

Duane Retraction Syndrome (DRS) is a congenital eye movement disorder that limits the ability of the eye to move outward toward the ear (abduction) and, in some cases, also limits movement inward toward the nose (adduction). This condition is often associated with the CHN1 gene, and understanding its symptoms is crucial for early diagnosis and […]

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 […]

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 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 […]

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 […]