Literature DB >> 454265

Fenestrated sheen macular dystrophy. A new autosomal dominant maculopathy.

F E O'Donnell, R B Welch.   

Abstract

A new, slowly progressive, autosomal dominant macular dystrophy was found in five patients from three generations of a family, with follow-up for long as 27 years. The mild functional abnormalities of this dystrophy were roughly correlated with age; in the sixth decade of life, paracentral scotomatous areas were noted. The earliest ophthalmoscopic findings were present in a 4-year-old and consisted of a yellowish refractile sheen with red fenestrations within the sensory retina of the macula. By the third decade, an annular zone of hypopigmentation of the retinal pigment epithelium (RPE) appeared around the area of the sheen and progressively enlarged. Surrounding the annular zone of hypopigmentation and at its center was slightly hyperpigmented RPE (bull's-eye lesion). Fluorescein angiography showed no abnormalities in the sensory retina and intact perfusion of choriocapillaris.

Entities:  

Mesh:

Year:  1979        PMID: 454265     DOI: 10.1001/archopht.1979.01020020034007

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  5 in total

1.  [Maculopathy with areolar retinal pigment epithelium defects].

Authors:  A S Bernd; B Voykov; E Zrenner
Journal:  Ophthalmologe       Date:  2010-10       Impact factor: 1.059

2.  The PROM1 mutation p.R373C causes an autosomal dominant bull's eye maculopathy associated with rod, rod-cone, and macular dystrophy.

Authors:  Michel Michaelides; Marie-Claire Gaillard; Pascal Escher; Leila Tiab; Matthew Bedell; François-Xavier Borruat; Daniel Barthelmes; Ruben Carmona; Kang Zhang; Edward White; Michelle McClements; Anthony G Robson; Graham E Holder; Keith Bradshaw; David M Hunt; Andrew R Webster; Anthony T Moore; Daniel F Schorderet; Francis L Munier
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-04-14       Impact factor: 4.799

3.  Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa.

Authors:  J R Heckenlively
Journal:  Br J Ophthalmol       Date:  1982-01       Impact factor: 4.638

4.  A detailed study of the phenotype of an autosomal dominant cone-rod dystrophy (CORD7) associated with mutation in the gene for RIM1.

Authors:  M Michaelides; G E Holder; D M Hunt; F W Fitzke; A C Bird; A T Moore
Journal:  Br J Ophthalmol       Date:  2005-02       Impact factor: 4.638

5.  ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy.

Authors:  M Michaelides; L L Chen; M A Brantley; J L Andorf; E M Isaak; S A Jenkins; G E Holder; A C Bird; E M Stone; A R Webster
Journal:  Br J Ophthalmol       Date:  2007-12       Impact factor: 4.638

  5 in total

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