AIM: Description of corneal findings in Fabry disease-related keratopathy using in vivo confocal microscopy. OBSERVATION: A 65-year-old man presenting with a cerebral ischemic lesion was referred to our clinic for ophthalmologic evaluation with a suspicion of inaugural Fabry disease. Slit lamp biomicroscopy showed whorl-like lines in the inferior cornea of both eyes. In vivo confocal microscopy revealed the presence of numerous hyperreflective intracellular inclusions in the corneal epithelium and stroma. DISCUSSION: The whorl-like lines are related to deposition and accumulation of glycosphingolipids in the epithelial and stromal layers of the cornea. This case is also interesting for the late manifestation of Fabry disease, showing the va...
WOS: 000396408900010PubMed ID: 28337063Fabry disease is a hereditary, X-linked lysosomal storage dis...
We report the clinical and confocal microscopic findings of the cornea in a patient with smouldering...
Purpose: To describe corneal microstructural modifications in an early case of Terrien marginal dege...
To compare the diagnostic power of slit-lamp examination with the in vivo corneal confocal microscop...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by the deficient activity of...
Neuropathy is a cause of significant disability in patients with Fabry disease, yet its diagnosis is...
ABSTRACT: Neuropathy is a cause of significant disability in patients with Fabry disease, yet its di...
PURPOSE: To report an advanced case of Terrien marginal corneal degeneration (TMD) analyzed by means...
International audiencePURPOSE: To report a novel finding in patients with Fabry disease, that is, th...
La enfermedad de Fabry es un raro trastorno ligado al cromosoma X causado por deficiencia de la enzi...
Purpose: To report corneal abnormalities and confocal microscopy findings in a patient with a varian...
PURPOSE:This study aims to assess the evolution of ocular manifestations in a cohort of Fabry patien...
Screening for Fabry disease (FD) increasingly reveals individuals without characteristic features an...
Purpose To apply in vivo corneal confocal microscopy (IVCM) to study the pathogenesis of keratitis (...
There is an evolution in the demands of modern ophthalmology from descriptive findings to assessment...
WOS: 000396408900010PubMed ID: 28337063Fabry disease is a hereditary, X-linked lysosomal storage dis...
We report the clinical and confocal microscopic findings of the cornea in a patient with smouldering...
Purpose: To describe corneal microstructural modifications in an early case of Terrien marginal dege...
To compare the diagnostic power of slit-lamp examination with the in vivo corneal confocal microscop...
Fabry disease (FD) is a rare X-linked lysosomal storage disorder caused by the deficient activity of...
Neuropathy is a cause of significant disability in patients with Fabry disease, yet its diagnosis is...
ABSTRACT: Neuropathy is a cause of significant disability in patients with Fabry disease, yet its di...
PURPOSE: To report an advanced case of Terrien marginal corneal degeneration (TMD) analyzed by means...
International audiencePURPOSE: To report a novel finding in patients with Fabry disease, that is, th...
La enfermedad de Fabry es un raro trastorno ligado al cromosoma X causado por deficiencia de la enzi...
Purpose: To report corneal abnormalities and confocal microscopy findings in a patient with a varian...
PURPOSE:This study aims to assess the evolution of ocular manifestations in a cohort of Fabry patien...
Screening for Fabry disease (FD) increasingly reveals individuals without characteristic features an...
Purpose To apply in vivo corneal confocal microscopy (IVCM) to study the pathogenesis of keratitis (...
There is an evolution in the demands of modern ophthalmology from descriptive findings to assessment...
WOS: 000396408900010PubMed ID: 28337063Fabry disease is a hereditary, X-linked lysosomal storage dis...
We report the clinical and confocal microscopic findings of the cornea in a patient with smouldering...
Purpose: To describe corneal microstructural modifications in an early case of Terrien marginal dege...