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Appl Immunohistochem Mol Morphol ; 31(10): 682-689, 2023.
Article in English | MEDLINE | ID: mdl-37751235

ABSTRACT

Corneal dystrophies are hereditary diseases affecting the corneal tissue; they are bilateral, symmetrical and unrelated to environmental or systemic conditions. Congenital corneal stromal dystrophy is a very rare autosomal dominant dystrophy that is caused by a mutation in the DCN gene that encodes decorin (a proteoglycan of the extracellular matrix). We herein report 4 cases of congenital stromal corneal dystrophy in 2 families, highlighting the previously undescribed histopathologic features, the possible differential diagnosis of this entity and the key role played by decorin staining in its diagnosis.


Subject(s)
Corneal Dystrophies, Hereditary , Humans , Decorin/genetics , Corneal Dystrophies, Hereditary/diagnosis , Corneal Dystrophies, Hereditary/genetics , Corneal Dystrophies, Hereditary/pathology , Mutation , Extracellular Matrix/pathology
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