ICE syndrome Irrigating IOL--endothelial touch PPMD solutions toxicity Toxic anterior Pseudoexfoliation Excessive use segment syndrome Hard cataract of phaco power Raised intraocular Chronic uveitis Intracameral pressure Chronic angle-closure drugs toxicity Chronic inflammation glaucoma DMD Brown McLean Trauma to corneal IOL-related syndrome endothelium factors Wound leak/shallow chamber/hypotony CHED: Congenital hereditary endothelial dystrophy, FECD: Fuchs endothelial
corneal dystrophy, ICE: Iridocorneal endothelial, PPMD: Posterior polymorphous endothelial dystrophy, IOL: Intraocular lens
Among the SCDs, Granular
corneal dystrophy and Macular
corneal dystrophy are more frequent as compared to other stromal dystrophies.1 A retrospective analysis was performed between November 2014 and July 2015 on all SCD patients visiting LRBT, General Hospital and Mughal Eye Hospital from Lahore during their ophthalmic consultation.
Although Crawford (5) had reported a case of concurrent granular
corneal dystrophy (GCD) and RP with autosomal dominant inheritance in a 58-year-old Korean woman, we present the first report of simultaneous MCD and RP.
Kinoshita, "Rho-associated kinase inhibitor eye drop treatment as a possible medical treatment for Fuchs
corneal dystrophy," Cornea, vol.
Matias-Guiu, "Lattice
corneal dystrophy type II: clinical, pathologic, and molecular study in a Spanish family," European Journal of Ophthalmology, vol.
PC-2 or Jackson-Lawler syndrome is characterized by natal or prenatal teeth (15-50%), numerous steatocystomas and various other cystic lesions (25%), hair abnormalities (9-25%), and
corneal dystrophy (8%), in addition to clinical features of PC-1 but with less severe keratodermas.9
Objective: The aim was to compare the corneal topography and tomography parameters of macular
corneal dystrophy (MCD) granular
corneal dystrophy (GCD) and lattice
corneal dystrophy (LCD) patients obtained by Scheimpflug imaging system.
Overall, our novel approach of combined EK and MICS can be performed for patients with Fuchs'
corneal dystrophy and dense cataract.
Matilda was aged 18 months when she was formally diagnosed with the
corneal dystrophy.
This edition includes new tables; new imaging techniques like ultrasound biomicroscopy and optical coherence tomography; and new entities like familial anterior-segment dysgenesis syndrome, diffuse keratoconjunctival proliferation, and new corneal dystrophies like zipper cell endotheliopathy, Lisch dystrophy, epithelial recurrent erosion dystrophy, subepithelial mucinous
corneal dystrophy, and dystrophia Helsinglandica and dystrophia Smolandiendsis.
M2 PHARMA-August 1, 2014-Haag-Streit UK to distribute Avellino Lab USA's genetic test for Granular
Corneal Dystrophy in UK