Literature DB >> 7091261

The frequency of posterior subcapsular cataract in the hereditary retinal degenerations.

J Heckenlively.   

Abstract

I analyzed the frequency and severity of posterior subcapsular cataracts in 291 patients with various forms of hereditary retinal degeneration, including typical retinitis pigmentosa (rod-cone degeneration), cone-rod degeneration, Usher's syndrome, and choroideremia. The overall frequency of posterior subcapsular cataract was 41%, less than generally thought. Posterior subcapsular cataracts were least common in cone-rod degeneration, and most common in the group with autosomal dominant retinitis pigmentosa. Only in the group with sporadic retinitis pigmentosa was a significant sex preference noted; females were affected more often (P less than or equal to .002). Severity was related to age of the patient and duration of disease in those affected. Posterior subcapsular cataract formation is unlikely to be an intrinsic expression of the various genes of hereditary retinal degeneration.

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Year:  1982        PMID: 7091261     DOI: 10.1016/0002-9394(82)90469-x

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  18 in total

1.  Retinal vessel oxygen saturation and vessel diameter in retinitis pigmentosa at various ages.

Authors:  Yao Zong; Leilei Lin; Changxian Yi; Xia Huang; Yue Fu; Yanmin Dong; Xiaobing Qian; Yujie Li; Qianying Gao
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2015-05-08       Impact factor: 3.117

2.  Radiotherapy for subfoveal neovascularisation associated with pathological myopia: a pilot study.

Authors:  H Kobayashi; K Kobayashi
Journal:  Br J Ophthalmol       Date:  2000-07       Impact factor: 4.638

3.  Outcome of cataract surgery in patients with retinitis pigmentosa.

Authors:  H Jackson; D Garway-Heath; P Rosen; A C Bird; S J Tuft
Journal:  Br J Ophthalmol       Date:  2001-08       Impact factor: 4.638

4.  Ciliary neurotrophic factor (CNTF) for human retinal degeneration: phase I trial of CNTF delivered by encapsulated cell intraocular implants.

Authors:  Paul A Sieving; Rafael C Caruso; Weng Tao; Hanna R Coleman; Darby J S Thompson; Keri R Fullmer; Ronald A Bush
Journal:  Proc Natl Acad Sci U S A       Date:  2006-02-27       Impact factor: 11.205

5.  Retinitis pigmentosa: clinical observations and correlations.

Authors:  R C Pruett
Journal:  Trans Am Ophthalmol Soc       Date:  1983

Review 6.  Ocular findings in a form of retinitis pigmentosa with a rhodopsin gene defect.

Authors:  E L Berson
Journal:  Trans Am Ophthalmol Soc       Date:  1990

7.  Correlations between electroretinography, morphology and function in retinitis pigmentosa.

Authors:  M Fahle; K P Steuhl; E Aulhorn
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1991       Impact factor: 3.117

8.  Posterior chamber intraocular lens implantation in patients with retinitis pigmentosa.

Authors:  R Reccia; A Scala; G Bosone
Journal:  Doc Ophthalmol       Date:  1989-06       Impact factor: 2.379

Review 9.  [Usher syndrome: clinical features, diagnostic options, and therapeutic prospects].

Authors:  M W Seeliger; M D Fischer; M Pfister
Journal:  Ophthalmologe       Date:  2009-06       Impact factor: 1.059

10.  Prevalence of posterior subcapsular lens opacities in patients with retinitis pigmentosa.

Authors:  G A Fishman; R J Anderson; P Lourenco
Journal:  Br J Ophthalmol       Date:  1985-04       Impact factor: 4.638

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