Coexistence of Meesmann Corneal Dystrophy and a Pseudo-Unilateral Lattice Corneal Dystrophy in a Patient With a Novel Pathogenic Variant in the Keratin K3 Gene: A Case Report

PURPOSE: This study aims to clinically and genetically report a case of coexisting Meesmann corneal dystrophy (MECD) and pseudo-unilateral lattice corneal dystrophy (LCD). METHODS: Clinical characterization was supported by a complete ophthalmological evaluation, including visual acuity measurement...

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Detalles Bibliográficos
Autores principales: Abad-Morales, Víctor, Barbany, Miriam, Gris, Oscar, Güell, José Luis, Pomares, Esther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cornea 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861493/
https://www.ncbi.nlm.nih.gov/pubmed/33346999
http://dx.doi.org/10.1097/ICO.0000000000002620

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7861493/
https://www.ncbi.nlm.nih.gov/pubmed/33346999
http://dx.doi.org/10.1097/ICO.0000000000002620

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