Genetics reference · Ophthalmology
Meesmann corneal dystrophy
MedlinePlus Genetics, National Library of Medicine · Retrieved 2026-10-13
Meesmann corneal dystrophy is an eye disease that affects the cornea, which is the clear front covering of the eye. This condition is characterized by the formation of tiny round cysts in the outermost layer of the cornea, called the corneal epithelium. This part of the cornea acts as a barrier to help prevent foreign materials, such as dust and bacteria, from entering the eye. In people with Meesmann corneal dystrophy, cysts can appear as early as the first year of life.…
Reference details
- Inheritance patterns
- Autosomal dominant
- Other names
- Corneal dystrophy, juvenile epithelial of Meesmann; Corneal dystrophy, Meesmann epithelial; Juvenile hereditary epithelial dystrophy; MECD; Meesman's corneal dystrophy; Meesmann corneal epithelial dystrophy; Meesmann epithelial corneal dystrophy
- NLM review date
- 2012-08
- NLM publication date
- 2020-08-18
Description
Sources and reuse
Original source summary. Follow the source links for additional information.
Source date: 2012-08. Retrieved: 2026-10-13. Text has been organized for reading; this import has not been independently reviewed by a clinician. It is not individualized medical advice.
Courtesy of the U.S. National Library of Medicine. DrugChat is independent and is not endorsed by NLM.