Literature DB >> 14652768

Coats-like lesions in Usher syndrome type II.

Hayyam Kiratli1, Cem Oztürkmen.   

Abstract

BACKGROUND: An unusual case of Usher syndrome type II associated with bilateral Coats-like exudative retinopathy is described.
METHODS: A 14-year-old boy with congenital sensorineural deafness and normal vestibular functions presented with a recent history of night blindness. He was followed for 3 years with fundus photography, intravenous fluorescein angiography, electroretinography and audiometric testings. His parents refused any form of treatment.
RESULTS: Fundoscopy showed bilateral retinitis pigmentosa and a single focus of subretinal exudation and overlying telangiectatic retinal vessels inferotemporal to the vascular arcade in the right eye. He had bilateral mild macular edema. A year later, a similar lesion developed inferotemporally in the left fundus. Electroretinography responses, particularly the rod-mediated signals, were significantly reduced. Audiometric studies documented hearing loss in high frequencies. His visual acuity declined from 20/40 to 20/80 RE and from 20/80 to 20/100 LE during follow-up. No new lesions developed.
CONCLUSIONS: Coats-type exudative lesions may develop in patients with Usher syndrome type II. Although left untreated, only a minimal increase in exudation occurred over 3 years.

Entities:  

Mesh:

Year:  2003        PMID: 14652768     DOI: 10.1007/s00417-003-0818-2

Source DB:  PubMed          Journal:  Graefes Arch Clin Exp Ophthalmol        ISSN: 0721-832X            Impact factor:   3.117


  8 in total

1.  Usher syndrome clinical types I and II: could ocular symptoms and signs differentiate between the two types?

Authors:  Ekaterini T Tsilou; Benjamin I Rubin; Rafael C Caruso; George F Reed; Anita Pikus; James F Hejtmancik; Fumino Iwata; Joy B Redman; Muriel I Kaiser-Kupfer
Journal:  Acta Ophthalmol Scand       Date:  2002-04

2.  Usher syndrome in the city of Birmingham--prevalence and clinical classification.

Authors:  C I Hope; S Bundey; D Proops; A R Fielder
Journal:  Br J Ophthalmol       Date:  1997-01       Impact factor: 4.638

3.  Retinitis pigmentosa: clinical observations and correlations.

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

4.  Usher's syndrome. Ophthalmic and neuro-otologic findings suggesting genetic heterogeneity.

Authors:  G A Fishman; A Kumar; M E Joseph; N Torok; R J Anderson
Journal:  Arch Ophthalmol       Date:  1983-09

5.  Coats-type retinitis pigmentosa in a 4-year-old child.

Authors:  R Y Kim; J J Kearney
Journal:  Am J Ophthalmol       Date:  1997-12       Impact factor: 5.258

6.  Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIa.

Authors:  M D Weston; J D Eudy; S Fujita; S Yao; S Usami; C Cremers; J Greenberg; R Ramesar; A Martini; C Moller; R J Smith; J Sumegi; W J Kimberling; J Greenburg
Journal:  Am J Hum Genet       Date:  2000-03-22       Impact factor: 11.025

Review 7.  Coats'-type retinitis pigmentosa.

Authors:  J A Khan; C H Ide; M P Strickland
Journal:  Surv Ophthalmol       Date:  1988 Mar-Apr       Impact factor: 6.048

  8 in total
  2 in total

1.  Coats-like Exudative Vitreoretinopathy in Retinitis Pigmentosa: Ocular Manifestations and Treatment Outcomes.

Authors:  Omar Moinuddin; Sanjana Sathrasala; K Thiran Jayasundera; Kari H Branham; Emmanuel Y Chang; Cynthia X Qian; Franco M Recchia; Abigail T Fahim; Cagri G Besirli
Journal:  Ophthalmol Retina       Date:  2020-04-09

Review 2.  Retinal Dystrophies and the Road to Treatment: Clinical Requirements and Considerations.

Authors:  Mays Talib; Camiel J F Boon
Journal:  Asia Pac J Ophthalmol (Phila)       Date:  2020 May-Jun
  2 in total

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