Open AccessCoexistence 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
Author(s) -
Víctor Abad–Morales,
Míriam Barbany,
Óscar Gris,
José L. Gϋell,
Esther Pomares
Publication year - 2020
Publication title -
cornea
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.274
H-Index - 117
eISSN - 1536-4798
pISSN - 0277-3740
DOI - 10.1097/ico.0000000000002620
Subject(s) - keratoconus , exome sequencing , phenotype , dystrophy , gene , medicine , visual acuity , genetics , cornea , ophthalmology , biology , pathology
This study aims to clinically and genetically report a case of coexisting Meesmann corneal dystrophy (MECD) and pseudo-unilateral lattice corneal dystrophy (LCD).