Corneal changes are frequently associated with X-linked ichthyosis. We present the first ultrastructural study of posterior stromal and pre-Descemet membrane changes in X-linked ichthyosis. A histopathological and ultrastructural study was performed on a corneal button from a 64-year-old man. Examination revealed a thick amorphous subepithelial material composed of proteinaceous material, disorganized collagen fibers, and electron-dense granular material. Numerous round and elongated empty spaces, some containing polymorphic and lamellated electron-dense material, were present along the anterior aspect of the Descemet membrane and throughout the stroma. These changes resemble those seen in lecithin cholesterol acyltransferase disease and ma...
We investigated an individual macular corneal dystrophy (MCD) type II cornea from a 42-year-old woma...
Type I mucopolysaccharidoses (MPS I) include three autosomal recessive disorders (Hurler, MPS IH; Sc...
We examined seven corneas from five patients with a new form of lattice corneal dystrophy (designate...
We carried out ophthalmological examinations, and histopathological examinations of skin biopsies in...
The authors report on the occurrence of ocular abnormalities in X-linked ichthyosis (XLI) patients, ...
blasts, and leukocytes of patienits with recessive x-linked ichthyosis. This study was uiidertaken t...
Congenital ichthyosiform erythroderma (CIE) and classic lamellar ichthyosis (LI) are autosomal reces...
Deficiency of lecithin:cholesterol acyltransferase, LCAT disease, is one of the dyslipoproteinemias ...
Abstract The human cornea was studied by using transmission and scanning electron microscopic techni...
Purpose: Collagen fibrils in the corneal stroma in macular corneal dystrophy, on average, are more c...
Processes that modulate the regular architecture and, hence, transparency of the cornea are poorly u...
We report on 2 cases of granular dystrophy (Groenouw type I). We studied the nature and the ultrastr...
Purpose. We report an investigation into the distribution of proteoglycans (PGs) in normal, organ-cu...
Using a high-intensity synchrotron X-ray source, the structural changes occurring in the corneal str...
Most patients with autosomal recessive lamellar ichthyosis are known to have markedly impaired skin ...
We investigated an individual macular corneal dystrophy (MCD) type II cornea from a 42-year-old woma...
Type I mucopolysaccharidoses (MPS I) include three autosomal recessive disorders (Hurler, MPS IH; Sc...
We examined seven corneas from five patients with a new form of lattice corneal dystrophy (designate...
We carried out ophthalmological examinations, and histopathological examinations of skin biopsies in...
The authors report on the occurrence of ocular abnormalities in X-linked ichthyosis (XLI) patients, ...
blasts, and leukocytes of patienits with recessive x-linked ichthyosis. This study was uiidertaken t...
Congenital ichthyosiform erythroderma (CIE) and classic lamellar ichthyosis (LI) are autosomal reces...
Deficiency of lecithin:cholesterol acyltransferase, LCAT disease, is one of the dyslipoproteinemias ...
Abstract The human cornea was studied by using transmission and scanning electron microscopic techni...
Purpose: Collagen fibrils in the corneal stroma in macular corneal dystrophy, on average, are more c...
Processes that modulate the regular architecture and, hence, transparency of the cornea are poorly u...
We report on 2 cases of granular dystrophy (Groenouw type I). We studied the nature and the ultrastr...
Purpose. We report an investigation into the distribution of proteoglycans (PGs) in normal, organ-cu...
Using a high-intensity synchrotron X-ray source, the structural changes occurring in the corneal str...
Most patients with autosomal recessive lamellar ichthyosis are known to have markedly impaired skin ...
We investigated an individual macular corneal dystrophy (MCD) type II cornea from a 42-year-old woma...
Type I mucopolysaccharidoses (MPS I) include three autosomal recessive disorders (Hurler, MPS IH; Sc...
We examined seven corneas from five patients with a new form of lattice corneal dystrophy (designate...