Results 141 to 150 of about 19,859 (195)
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Corneal opacities in gaucher disease

American Journal of Ophthalmology, 1998
To describe the corneal findings in a variant of Gaucher disease.Case report. In an 18-year-old man, ophthalmic and general clinical evaluation, and enzymatic and molecular genetics studies were performed.Diffuse, well-defined, small, linear, or dotlike corneal opacities were observed through, out the posterior two thirds of the corneal stroma in both ...
A, Guemes   +5 more
openaire   +2 more sources

Corneal Transplants for the Treatment of Congenital Corneal Opacities

Journal of Pediatric Ophthalmology & Strabismus, 2005
Purpose: To describe the results of corneal transplants in infants and young children with congenital corneal disorders. Methods: The charts of 38 children who underwent corneal transplantation for congenital corneal opacities from 1988 to 1999 at the Hospital for Sick Children ...
Adi, Michaeli   +2 more
openaire   +2 more sources

Corneal Opacities in the Hallermann-Streiff Syndrome

Ophthalmic Genetics, 2008
We present six patients with typical Hallermann-Streiff syndrome. All have microphthalmia and were operated for congenital cataract. Three of the patients developed a severe glaucoma and one patient presented repeated uveal effusions. Five of our patients have the same pattern of corneal stromal opacities.
Roulez, Françoise   +2 more
openaire   +3 more sources

Corneal opacities secondary to Viscoat®

Journal of Cataract and Refractive Surgery, 1986
Viscoat is a new viscoelastic solution of chondroitin sulfate and sodium hyaluronate dissolved in a phosphate buffer. Recent findings of postoperative corneal deposits in association with its use have been reported to Cilco. The corneal deposits are noted 18 to 48 hours postoperatively and are similar in appearance to calcific band keratopathy.
S, Ullman   +2 more
openaire   +2 more sources

[Corneal opacity].

Klinische Monatsblatter fur Augenheilkunde, 1986
A case with bilateral corneal opacification in the form of a half-ring is described. Routine laboratory tests revealed no abnormalities, and serum lipoprotein composition was normal. The authors suspect that this was a case of primary lipoidal keratopathy.
E C, van Pampus   +4 more
openaire   +1 more source

Corneal Opacities in the Neonate

NeoReviews, 2018
A congenital corneal opacity is a rare occurrence but can cause significant visual compromise to the affected infant. Corneal opacities can arise from infectious, metabolic, genetic, developmental, and idiopathic causes. Early diagnosis is imperative so that an appropriate treatment plan can be initiated as soon as possible to obtain the best visual ...
openaire   +1 more source

AN UNUSUAL CORNEAL OPACITY

Archives of Ophthalmology, 1931
This case of opacity of the cornea is reported because of its rarity and its obscure nature and origin. The opacity was confined to the anterior layers of the substantia propria. It had the appearance of a "snow-storm" when looked at with focal illumination, and consisted of grayish-white round dots under the slit-lamp.
openaire   +1 more source

Herpetic Corneal Opacities

2020
Corneal infection by Herpes Simplex Virus (HSV) and its recurrences may induce loss of transparency and regularity of shape causing loss of vision. Virus replication at the corneal epithelium and immunologic response to virus antigens retained within the stroma are responsible for the inflammatory process that leads to corneal destruction with ...
openaire   +2 more sources

Oversized corneal grafts for corneal opacities with iridocorneal adhesions

Ophthalmology, 2001
To evaluate the efficacy of 1-mm oversized corneal grafts in patients with acquired corneal opacities and extensive peripheral iridocorneal adhesions.Prospective noncomparative case series.Twenty patients (20 eyes) aged 15 years or older with unilateral or bilateral corneal opacification and a shallow anterior chamber.Penetrating keratoplasty was ...
R B, Vajpayee   +5 more
openaire   +2 more sources

Corneal Opacities in Spondyloepiphyseal Dysplasia Tarda

Cornea, 1994
Spondyloepiphyseal dysplasia tarda is an inherited skeletal dysplasia involving the spine and epiphyses of long bones with onset in childhood, giving rise to disproportionate short stature and degenerative spine and hip disease. Associated ocular disease is not commonly recognized.
J A, Wells   +3 more
openaire   +2 more sources

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