Literature DB >> 8719692

Familial exudative vitreoretinopathy.

W E Benson.   

Abstract

PURPOSE: To evaluate the natural history of Familial Exudative Vitreoretinopathy (FEVR) with emphasis on the effect of the age of onset on its severity and on the development of late complications such as cataract and retinal detachment. Also, to evaluate affected patients for DNA abnormalities.
METHODS: The records of thirty-nine patients with FEVR were studied. All were asked to come in for a final follow-up examination. The referring physician was asked to provide the latest findings for those who could not. On 10 patients, karyotypes were prepared.
RESULTS: Only 2 of 28 patients whose onset of symptoms was prior to their third birthday had a final visual acuity of 20/200 or better. Older patients had a better prognosis, because they were more likely to have asymmetrical retinal deterioration with only one eye deteriorating. Preservation of good visual acuity into the teens and later was no guarantee that deterioration would not occur. In 3 eyes of 4 patients who were asymptomatic until 15 years of age, the final visual acuity was counting fingers or worse. In 5 patients, retinal detachment developed 6 to 17 years after apparent stabilization. The karyotype of 10 patients showed no evidence for rearrangement, altered size, translocations or deletions of chromosome 11 or any other chromosome. Of the 31 eyes in patients older than 15 years, 10 (32%) had a significant cataract. Three eyes underwent cataract surgery.
CONCLUSIONS: The prognosis for infants with FEVR is extremely poor and the long-term prognosis for patients with a later onset of the condition is guarded. Retinal detachment, macular dragging, and cataract are common late complications which can develop even in patients whose eye findings appear to be stable. Karyotype studies ruled out involvement of chromosome 11 or others at a gross level, but did not exclude them at the location for some genetic defect related to FEVR because single base changes and small deletions or insertions may be undetectable by the methods utilized.

Entities:  

Mesh:

Year:  1995        PMID: 8719692      PMCID: PMC1312071     

Source DB:  PubMed          Journal:  Trans Am Ophthalmol Soc        ISSN: 0065-9533


  72 in total

1.  X-linked congenital retinoschisis.

Authors:  U Kellner; S Brümmer; M H Foerster; A Wessing
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1990       Impact factor: 3.117

2.  Laser photocoagulation for stage 3+ retinopathy of prematurity.

Authors:  J A McNamara; W Tasman; G C Brown; J L Federman
Journal:  Ophthalmology       Date:  1991-05       Impact factor: 12.079

3.  Unusual manifestations of X-linked retinoschisis.

Authors:  C M Greven; R J Moreno; W Tasman
Journal:  Trans Am Ophthalmol Soc       Date:  1990

4.  Treatment of retinopathy of prematurity with argon laser photocoagulation.

Authors:  M B Landers; C A Toth; H C Semple; L S Morse
Journal:  Arch Ophthalmol       Date:  1992-01

5.  Nasal retinal dragging in X-linked retinoschisis.

Authors:  W Tasman; C Greven; R Moreno
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1991       Impact factor: 3.117

6.  Management of late-onset angle-closure glaucoma associated with retinopathy of prematurity.

Authors:  A J Michael; S R Pesin; L J Katz; W S Tasman
Journal:  Ophthalmology       Date:  1991-07       Impact factor: 12.079

7.  Signs, complications, and platelet aggregation in familial exudative vitreoretinopathy.

Authors:  C E van Nouhuys
Journal:  Am J Ophthalmol       Date:  1991-01-15       Impact factor: 5.258

8.  Transscleral and indirect ophthalmoscope diode laser retinal photocoagulation: experimental quantification of the therapeutic range for their application in the treatment of retinopathy of prematurity.

Authors:  A Obana; B Lorenz; R Birngruber
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-07       Impact factor: 3.117

9.  Late traction detachment in retinopathy of prematurity or ROP-like cases.

Authors:  R Machemer
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-07       Impact factor: 3.117

10.  Scleral buckling surgery for stage 4B retinopathy of prematurity.

Authors:  S W Noorily; K Small; E de Juan; R Machemer
Journal:  Ophthalmology       Date:  1992-02       Impact factor: 12.079

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  29 in total

1.  [Criswick-Schepens syndrome -- familial exudative vitreoretinopathy. Report of six cases in two consanguineous families].

Authors:  A Alsheikheh; W Lieb; F Grehn
Journal:  Ophthalmologe       Date:  2004-09       Impact factor: 1.059

2.  [Familial exudative vitreoretinopathy].

Authors:  D Finis; J Stammen; A M Joussen
Journal:  Ophthalmologe       Date:  2010-07       Impact factor: 1.059

3.  Reduced bone mineral density and hyaloid vasculature remnants in a consanguineous recessive FEVR family with a mutation in LRP5.

Authors:  L M Downey; H M Bottomley; E Sheridan; M Ahmed; D F Gilmour; C F Inglehearn; A Reddy; A Agrawal; J Bradbury; C Toomes
Journal:  Br J Ophthalmol       Date:  2006-09       Impact factor: 4.638

4.  25-gauge lens-sparing vitrectomy with dissection of retrolental adhesions on the peripheral retina for familial exudative vitreoretinopathy in infants.

Authors:  Jin Ma; Yin Hu; Lin Lu; Xiaohu Ding
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2018-06-16       Impact factor: 3.117

5.  Macular Microvascular Findings in Familial Exudative Vitreoretinopathy on Optical Coherence Tomography Angiography.

Authors:  S Tammy Hsu; Avni P Finn; Xi Chen; Hoan T Ngo; Robert J House; Cynthia A Toth; Lejla Vajzovic
Journal:  Ophthalmic Surg Lasers Imaging Retina       Date:  2019-05-01       Impact factor: 1.300

Review 6.  The Norrin/Frizzled4 signaling pathway in retinal vascular development and disease.

Authors:  Xin Ye; Yanshu Wang; Jeremy Nathans
Journal:  Trends Mol Med       Date:  2010-08-03       Impact factor: 11.951

7.  Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree.

Authors:  C Toomes; L M Downey; H M Bottomley; H A Mintz-Hittner; C F Inglehearn
Journal:  Br J Ophthalmol       Date:  2005-02       Impact factor: 4.638

8.  Genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of the EVR1 locus on chromosome 11q in a large autosomal dominant pedigree.

Authors:  M A Bamashmus; L M Downey; C F Inglehearn; S R Gupta; D C Mansfield
Journal:  Br J Ophthalmol       Date:  2000-04       Impact factor: 4.638

9.  Pharmacologic Activation of Wnt Signaling by Lithium Normalizes Retinal Vasculature in a Murine Model of Familial Exudative Vitreoretinopathy.

Authors:  Zhongxiao Wang; Chi-Hsiu Liu; Ye Sun; Yan Gong; Tara L Favazza; Peyton C Morss; Nicholas J Saba; Thomas W Fredrick; Xi He; James D Akula; Jing Chen
Journal:  Am J Pathol       Date:  2016-08-12       Impact factor: 4.307

10.  Reactivation of Retinopathy of Prematurity in Adults and Adolescents.

Authors:  Ogul E Uner; Prethy Rao; G Baker Hubbard
Journal:  Ophthalmol Retina       Date:  2020-02-11
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