Purpose: To report corneal findings in a familial case of the crystalline subtype of pre-Descemetic corneal dystrophy. Case Report: A 19-year-old girl and her 44-year-old mother were found to have asymptomatic, bilateral, punctiform and multi-colored crystalline opacities across the whole posterior layer of the corneas. Endothelial specular microscopy revealed the presence of white round flecks located at different levels anterior to the endothelium. No systemic abnormalities or medications could be related to account for these findings. Conclusion: To the best of our knowledge, this is the third familial report of this rare corneal disorder. Differential diagnosis may include Schnyder corneal dystrophy, cystinosis, Bietti´s dystrophy and m...
Purpose: To report the microstructural features of Meesmann corneal dystrophy (MCD) in two patients....
Purpose: The aim of this study was to describe the morphology, corneal topography and sensitivity in...
Corneal dystrophy is kind Groenouw an autosomal recessive disease whose gene is located in 16q22. It...
The purpose of this paper is to report the first family from Great Britain with central crystalline ...
To present corneal confocal microscopy (CCM) findings in a series of patients with pre-Descemet corn...
Purpose: To report the observation of a triple corneal dystrophy association consisting of keratocon...
Abstract The term corneal dystrophy embraces a heterogenous group of bilateral genetically determine...
OBJECTIVE: To describe the phenotypic variation exhibited by members of families with combined granu...
Schnyder corneal crystalline dystrophy (SCCD) comprises corneal opacities often associated with prec...
Purpose: To describe the phenotype of an autosomal-dominant corneal dystrophy with an early onset of...
Purpose: To assess the findings, visual morbidity, and surgical intervention in Schnyder crystalline...
Purpose: Schnyder crystalline corneal dystrophy (SCCD) is an autosomal dominant disease characterize...
Abstract Background Corneal dystrophies are a group of rare, inherited disorders that are usually bi...
Bietti’s crystalline dystrophy (BCD) is a rare disease presenting with the appearance of intraretina...
PURPOSE: To report a new family belonging to a previously non-investigated geographic are a with...
Purpose: To report the microstructural features of Meesmann corneal dystrophy (MCD) in two patients....
Purpose: The aim of this study was to describe the morphology, corneal topography and sensitivity in...
Corneal dystrophy is kind Groenouw an autosomal recessive disease whose gene is located in 16q22. It...
The purpose of this paper is to report the first family from Great Britain with central crystalline ...
To present corneal confocal microscopy (CCM) findings in a series of patients with pre-Descemet corn...
Purpose: To report the observation of a triple corneal dystrophy association consisting of keratocon...
Abstract The term corneal dystrophy embraces a heterogenous group of bilateral genetically determine...
OBJECTIVE: To describe the phenotypic variation exhibited by members of families with combined granu...
Schnyder corneal crystalline dystrophy (SCCD) comprises corneal opacities often associated with prec...
Purpose: To describe the phenotype of an autosomal-dominant corneal dystrophy with an early onset of...
Purpose: To assess the findings, visual morbidity, and surgical intervention in Schnyder crystalline...
Purpose: Schnyder crystalline corneal dystrophy (SCCD) is an autosomal dominant disease characterize...
Abstract Background Corneal dystrophies are a group of rare, inherited disorders that are usually bi...
Bietti’s crystalline dystrophy (BCD) is a rare disease presenting with the appearance of intraretina...
PURPOSE: To report a new family belonging to a previously non-investigated geographic are a with...
Purpose: To report the microstructural features of Meesmann corneal dystrophy (MCD) in two patients....
Purpose: The aim of this study was to describe the morphology, corneal topography and sensitivity in...
Corneal dystrophy is kind Groenouw an autosomal recessive disease whose gene is located in 16q22. It...