About Schnyder Crystalline Corneal Dystrophy

Schnyder Corneal Dystrophy, also known as schnyder crystalline corneal dystrophy, is related to corneal dystrophy and keratopathy. An important gene associated with Schnyder Corneal Dystrophy is UBIAD1 (UbiA Prenyltransferase Domain Containing 1), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Platelet homeostasis. Affiliated tissues include eye, skin and spleen, and related phenotypes are corneal dystrophy and crystalline corneal dystrophy

Major Symptoms of Schnyder Crystalline Corneal Dystrophy

Schnyder crystalline corneal dystrophy is a rare genetic disorder characterized by the progressive degenerative changes in the cornea, leading to severe vision loss. The major symptoms include dry and crusty eyes, frequent infections, and corneal perforation.

Suitable Lifestyle for People with Schnyder Crystalline Corneal Dystrophy

Schnyder crystalline corneal dystrophy is a hereditary eye disease, and patients may be affected to varying degrees, including vision loss, eye pain, tearing, etc. However, the impact of lifestyle on eye disease is very small. Therefore, people suffering from Schnyder crystalline corneal dystrophy should follow the doctor's advice and pay attention to protecting eye health, such as maintaining good living habits, avoiding long-term use of electronic products, and maintaining adequate rest.

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