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GTR Home > Conditions/Phenotypes > Corneal dystrophy, Meesmann, 2

Corneal dystrophy, Meesmann, 2

Summary

Meesmann corneal dystrophy-2 (MECD2) is characterized by fragility of the anterior corneal epithelium and the presence of intraepithelial microcysts. Although the disease is generally mild and affected individuals are often asymptomatic, some suffer from recurrent erosions leading to lacrimation, photophobia, and deterioration in visual acuity (summary by Szaflik et al., 2008). For a discussion of genetic heterogeneity of Meesmann corneal dystrophy, see MECD1 (122100). [from OMIM]

Available tests

1 test is in the database for this condition.

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Clinical tests (1 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CK3, K3, MECD2, KRT3
    Summary: keratin 3

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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