Literature DB >> 26149492

[The diseased vitreous body: Malformations, developmental disorders and opacities].

Bernd Kirchhof1.   

Abstract

Remnants of a persistent hyaloid artery can occasionally cause cataracts and traction on the retina at the posterior pole of the eye.It is the task of the ophthalmologist to weigh up the risk of amblyopia against the risks of vitrectomy and lensectomy. The retina is primarily intact. This is different from the group of hereditary vitreoretinal dystrophies where defects in the retina and vitreous body contribute equally to the overall clinical manifestations. Familial exudative vitreoretinopathy (FEVR) of childhood is sometimes misdiagnosed as uveitis. Retinal exudates leak from enormously permeable retinal vessels and it is necessary to completely remove such abnormal vessels to stop progression. The peculiar vitreous opacities consist of paper-like veils which are stacked like onion skins. The FEVR simulates retinopathy of prematurity and other exudative vitreoretinopathies. Stickler and Wagner syndromes are associated with a high risk of rhegmatogenous retinal detachment, similar to giant retinal tears. Occasionally, extraocular manifestations, such as hyperextensive joints are indicative of a systemic connective tissue disease.The peripheral retina is mechanically weak and susceptible to tears and giant or multiple tears can occur. The prognosis is further aggravated by an elevated risk of proliferative vitreoretinopathy (PVR). It is, therefore, essential to identify the risk profile in this constellation and bear the risk of PVR in mind when selecting a treatment regimen, similar to that for giant tear retinal detachment.

Entities:  

Mesh:

Year:  2015        PMID: 26149492     DOI: 10.1007/s00347-015-0059-x

Source DB:  PubMed          Journal:  Ophthalmologe        ISSN: 0941-293X            Impact factor:   1.059


  10 in total

1.  Autosomal dominant rhegmatogenous retinal detachment--clinical appearance and surgical outcome.

Authors:  Thomas Theelen; Sioe Lie Go; Maurits A D Tilanus; B Jeroen Klevering; August F Deutman; Frans P M Cremers; Carel B Hoyng
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2004-04-02       Impact factor: 3.117

2.  Clinical presentation of familial exudative vitreoretinopathy.

Authors:  Tushar M Ranchod; Lawrence Y Ho; Kimberly A Drenser; Antonio Capone; Michael T Trese
Journal:  Ophthalmology       Date:  2011-08-25       Impact factor: 12.079

3.  Prevention of retinal detachment in Stickler syndrome: the Cambridge prophylactic cryotherapy protocol.

Authors:  Gregory S Fincham; Laura Pasea; Christopher Carroll; Annie M McNinch; Arabella V Poulson; Allan J Richards; John D Scott; Martin P Snead
Journal:  Ophthalmology       Date:  2014-05-01       Impact factor: 12.079

4.  Juvenile retinal detachment as a complication of familial exudative vitreoretinopathy.

Authors:  C E van Nouhuys
Journal:  Fortschr Ophthalmol       Date:  1989

5.  Profibrotic cytokines in aqueous humour correlate with aqueous flare in patients with rhegmatogenous retinal detachment.

Authors:  Robert Hoerster; Manuel M Hermann; Andre Rosentreter; Philipp S Muether; Bernd Kirchhof; Sascha Fauser
Journal:  Br J Ophthalmol       Date:  2013-01-26       Impact factor: 4.638

6.  Fellow eyes of giant retinal breaks.

Authors:  H M Freeman
Journal:  Trans Am Ophthalmol Soc       Date:  1978

7.  Rhegmatogenous retinal detachment after prophylactic argon laser photocoagulation.

Authors:  M Bonnet; P Aracil; F Carneau
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1987       Impact factor: 3.117

Review 8.  Advances in the management of congenital and infantile cataract.

Authors:  I C Lloyd; J Ashworth; S Biswas; R V Abadi
Journal:  Eye (Lond)       Date:  2007-10       Impact factor: 3.775

9.  Findings of perinatal ocular examination performed on 3573, healthy full-term newborns.

Authors:  Li-Hong Li; Na Li; Jun-Yang Zhao; Ping Fei; Guo-ming Zhang; Jian-bo Mao; Paul J Rychwalski
Journal:  Br J Ophthalmol       Date:  2013-02-20       Impact factor: 4.638

10.  Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes.

Authors:  Khanh-Nhat Tran-Viet; Vincent Soler; Valencia Quiette; Caldwell Powell; Tammy Yanovitch; Ravikanth Metlapally; Xiaoyan Luo; Nicholas Katsanis; Erica Nading; Terri L Young
Journal:  Mol Vis       Date:  2013-04-05       Impact factor: 2.367

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.