Cargando…
Alcohol epitheliectomy with mechanical debridement in a case of granular corneal dystrophy with r555w homozygous mutation of TGF B1 gene
An eight-year-old girl, an offspring of a consanguineous marriage presented with multiple anterior stromal geographic corneal opacities in both eyes. She was diagnosed to have superficial variant of granular dystrophy based on the family history, clinical features and mutation of TGF B1 gene. She wa...
Autores principales: | Garg, Prashant, Jabbar, Aneeta |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907037/ https://www.ncbi.nlm.nih.gov/pubmed/20534926 http://dx.doi.org/10.4103/0301-4738.64126 |
Ejemplares similares
-
The TGFBI R555W mutation induces a new granular corneal dystrophy type I phenotype
por: Zhu, Yanan, et al.
Publicado: (2011) -
Corneal Higher Order Aberrations in Granular, Lattice and Macular Corneal Dystrophies
por: Yagi-Yaguchi, Yukari, et al.
Publicado: (2016) -
Changes in Stress-Strain Index and Corneal Biomechanics in Granular Corneal Dystrophy
por: Heidari, Hamidreza, et al.
Publicado: (2022) -
A Homozygous Mutation in the TUB Gene Associated with Retinal Dystrophy and Obesity
por: Borman, Arundhati Dev, et al.
Publicado: (2014) -
Phenotypic Spectrum of Granular Corneal Dystrophy Type II in Two Italian Families Presenting an Unusual Granular Corneal Dystrophy Type I Clinical Appearance
por: Mazzotta, Cosimo, et al.
Publicado: (2015)