Literature DB >> 3931669

Pigment epithelial pattern dystrophy: a peripheral type.

J W Delleman, P T de Jong.   

Abstract

A hitherto undescribed form of pattern dystrophy of the retinal pigment epithelium was found in a patient suffering from mucopolysaccharidosis II or Hunter's disease. We propose the name peripheral pattern dystrophy.

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Year:  1985        PMID： 3931669      PMCID： PMC1040733          DOI： 10.1136/bjo.69.10.754

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN： 0007-1161            Impact factor:   4.638


  8 in total

1.  An unusual case of gargoylism.

Authors:  J M D HOOPER
Journal:  Guys Hosp Rep       Date:  1952

2.  [Corneal and retinal disorders associated with mucopolysaccharidosis (8 cases)].

Authors:  C Thomas; A Raspiller; M Fall
Journal:  Bull Soc Ophtalmol Fr       Date:  1970 Sep-Oct

Review 3.  Electroretinography and fundus oculi findings in Hurler's disease and allied mucopolysaccharidoses.

Authors:  J P Gills; R Hobson; W B Hanley; V A McKusick
Journal:  Arch Ophthalmol       Date:  1965-11

4.  Electrophysiological and psychophysical findings in Hunter syndrome.

Authors:  F A Abraham; S Yatziv; A Russell; E Auerbach
Journal:  Arch Ophthalmol       Date:  1974-03

5.  Pigment epithelial pattern dystrophy. Four different manifestations in a family.

Authors:  P T de Jong; J W Delleman
Journal:  Arch Ophthalmol       Date:  1982-09

6.  Further electroretinographic studies of patients with mucopolysaccharidoses.

Authors:  L S Leung; G W Weinstein; R R Hobson
Journal:  Birth Defects Orig Artic Ser       Date:  1971-03

7.  [Macroreticular and butterfly shaped dystrophies of the retinal pigment epithelium (author's transl)].

Authors:  P Girard; G Setbon; A Forest; G Coscas
Journal:  J Fr Ophtalmol       Date:  1980       Impact factor: 0.818

8.  Ocular histopathology in Hunter's syndrome. Systemic mucopolysaccharidosis type II.

Authors:  M F Goldberg; J R Duke
Journal:  Arch Ophthalmol       Date:  1967-04
  8 in total

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