Results 71 to 80 of about 152,878 (215)

Posterior amorphous corneal dystrophy caused by a de novo deletion

, 2017
We present a newborn diagnosed with posterior amorphous corneal dystrophy (PACD). PACD is a rare disorder with partial or complete posterior lamellar corneal opacification.
Odent, S., Casteels, Ingele, Devriendt, Koenraad, Dieltiëns, M., Catherine, Cassiman, Hua, M-T.   +5 more
core   +1 more source

Epidemiological and Histopathological Assessment of Corneal Dystrophies Leading to Corneal Transplantation [PDF]

, 2018
Purpose: To carry out an epidemiological assessment of corneal dystrophies leading to corneal transplantation and to determine different subtype frequencies.
Soleimani, Mohammad, Tabatabaei, Seyed Ali, Asadi-Amoli, Fahimeh, Mehrtash, Vahid, Hadi, Abdollah, Nozarian, Zohreh   +5 more
core   +1 more source

Progressive External Ophthalmoplegia and Lattice Corneal-Dystrophy

, 1992
The authors conducted a study in a family pedigree comprising 33 patients (men 16, women 17). In this pedigree there coexisted patients with progressive external ophthalmoplegia and corneal lattice dystrophy.
Kitsos, G., Asproudis, I., Psilas, K., Petroutsos, G., Melissourgos, I.   +4 more
core  

Recurrence of macular corneal dystrophy on the graft 50 years after penetrating keratoplasty

, 2020
Purpose: To report the recurrence of a macular corneal stromal dystrophy 50 years after penetrating keratoplasty (PKP).Methods: Observational case reportCase description: A 76-year-old male patient presented with visual impairment in the right eye ...
Hasenfus, A, Viestenz, A, Flockerzi, E, Schlötzer-Schrehardt, U, Matoula, P, Bischoff-Jung, M, Seitz, B   +6 more
core   +1 more source

In vivo laser confocal microscopy findings in patients with map-dot-fingerprint (epithelial basement membrane) dystrophy

Clinical Ophthalmology, 2012
Akira Kobayashi, Hideaki Yokogawa, Kazuhisa SugiyamaDepartment of Ophthalmology, Kanazawa University Graduate School of Medical Science, Kanazawa, JapanBackground: The purpose of this study was to investigate pathological changes of the corneal cell ...
Kobayashi A, Yokogawa H, Sugiyama K
doaj  

Combination of phototherapeutic keratectomy and wavefront-guided photorefractive keratectomy for the treatment of Thiel-Behnke corneal dystrophy

Indian Journal of Ophthalmology, 2017
Phototherapeutic keratectomy (PTK) has been used to treat anterior corneal dystrophy but may cause hyperopic shift or corneal high-order aberration.
Chia-Chieh Hsiao, Yu-Chih Hou
doaj   +1 more source

Melatonin protects against oxidative stress in granular corneal dystrophy type 2 corneal fibroblasts by mechanisms that involve membrane melatonin receptors

, 2011
Considering that oxidative stress plays a role in corneal fibroblast degeneration during granular corneal dystrophy type 2 (GCD2) and melatonin is an effective antioxidant, we examined the ability of melatonin to protect against oxidative stress-induced ...
김태임, 다다후자예프, 최승일, 김응권, 류현미   +4 more
core   +1 more source

Bilateral Terrien′s Marginal Degeneration and Posterior Polymorphous Dystrophy in a Patient with Rheumatoid Arthritis

Journal of Ophthalmic & Vision Research, 2012
Purpose: To report an interesting case of concomitant bilateral Terrien′s marginal degeneration-like corneal ectasia and posterior polymorphous corneal dystrophy in a young man with quiescent rheumatoid arthritis.
Siamak Zarei-Ghanavati, Mohammad-Ali Javadi, Shahin Yazdani   +2 more
doaj  

Reticular Bullous Epithelial Corneal Edema after Netarsudil Use for Elevated Intraocular Pressure with Concurrent Fuchs Endothelial Corneal Dystrophy: A Case Report

Case Reports in Ophthalmology
Introduction: We describe a case of reticular bullous corneal epithelial edema associated with the use of netarsudil ophthalmic solution (0.02%) for elevated intraocular pressure. Case Presentation: A 74-year-old man with a complex ocular medical history,
Kathryn S. Park, Alexander C. Lieu, Michael J. Ang, Natalie A. Afshari   +3 more
doaj   +1 more source

Late-Onset Lattice Corneal Dystrophy Associated TGFBI p.H626R Mutation in Members of a Canadian Family [PDF]

, 2019
Within the over 70 reported Transforming Growth factor – beta induced (TGFBI) Corneal Dystrophy mutations1, more than 40 are associated with Lattice Corneal Dystrophy (LCD), subtypes I, III, IIIA and IIIB according to Human Gene Mutation Database (HGMD®)
Chan, Carol, DeDionisio, Lawrence, McMullen, C. B. Tara, Chao-Shern, Connie, Nesbit, M. Andrew; id_orcid   +4 more
core   +1 more source