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pro vyhledávání: '"Ectopia lentis et pupillae"'
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Publikováno v:
Journal of pediatric ophthalmology and strabismus. 56
Ectopia lentis is displacement of the lens from its original position. It can be inherited or acquired with isolated or systemic findings. The authors describe a 4-year-old girl with isolated ectopia lentis et pupillae caused by pathogenic variants i
Publikováno v:
Ophthalmology. 105:1331-1336
Background Ectopia lentis et pupillae (ELeP) is a rare congenital inherited disorder characterized by lenticular and pupillary ectopia. Recent speculation on its pathogenesis is based on clinical observation and includes a neuroectodermal defect or p
Autor:
J.R.M. Cruysberg, A.J.L.G. Pinckers
Publikováno v:
British Journal of Ophthalmology, 79, 135-138
British Journal of Ophthalmology, 79, 2, pp. 135-138
British Journal of Ophthalmology, 79, pp. 135-138
British Journal of Ophthalmology, 79, 2, pp. 135-138
British Journal of Ophthalmology, 79, pp. 135-138
In nine members from three generations and in a distant relative, at least three significant characteristics of the ectopia lentis et pupillae syndrome were established including ectopia lentis, ectopia pupillae, persistent pupillary membrane, iris t
Publikováno v:
Journal of Medical Genetics. 28:791-794
Two sib pairs and a fifth child are described with autosomal recessive ectopia lentis et pupillae. Patients with this disorder need regular ophthalmic review, but do not have the skeletal and metabolic complications associated with other syndromes wi
Publikováno v:
Indian Journal of Ophthalmology, Vol 37, Iss 1, Pp 32-34 (1989)
A rare case of congenital bilateral ectopia lentis et pupillae (ELEP) is reported in a 32 year old female presenting with complaints of diminution of vision in both eyes. Associations of optic nerve hypoplasia and myelinated nerve fibers are being re
Externí odkaz:
https://doaj.org/article/858ddedaad084980ab40c43f90044d4a
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
A 52-year-old patient presented with signs clinically consistent with ectopia lentis et pupillae syndrome. The patient was treated successfully with vitrectomy, dislocated lens removal using perfluorocarbon liquid and phacofragmentation in the vitreo
Editor,—Congenital abnormalities of pupil position and shape are uncommon. Slit lamp examination will usually identify which of the various rare anterior segment developmental anomalies has caused the pupil appearance. Possible associations include
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75c7344142108293eb1deb6128a175ca
https://europepmc.org/articles/PMC1723246/
https://europepmc.org/articles/PMC1723246/
Publikováno v:
Graefe's Archive for Clinical and Experimental Ophthalmology. 244:878-879
To report a case of clinically unilateral congenital ectopia lentis et pupillae (ELeP) and discuss its surgical management. Interventional case report. A 37–year–old female was referred to our service for surgical management of unilateral ectopia
Publikováno v:
Eye. 17:243-244
This case report highlights the successful management, by vitrectomy alone, of a case of chronic phacolytic glaucoma secondary to a dislocated hypermature lens in the vitreous of a patient with ectopia lentis et pupillae (ELP). The features and compl