Literature DB >> 990013

Retinal functions in dominant cystoid macular dystrophy (DCMD).

A Pinckers, A F Deutman, J G Notting.   

Abstract

Dominant cystoid macular dystrophy (DCMD) occurred in 28 members of 5 unrelated families. The disease is characterized by cystoid macular oedema and leakage from retinal capillaries in the posterior pole. Colour vision examination reveals a type I red-green defect with concomitant blue-yellow defectiveness; the latter may be caused by the leaking capillaries. The ERG is normal. The EOG is subnormal. Darkadaptation curves are often slightly disturbed. There are frequently also aspecific pigmentary alterations in the peripheral fundus.

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Year:  1976        PMID: 990013     DOI: 10.1111/j.1755-3768.1976.tb01287.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN: 0001-639X


  5 in total

Review 1.  The incidence, pathogenesis and treatment of cystoid macular edema following cataract surgery.

Authors:  A J Flach
Journal:  Trans Am Ophthalmol Soc       Date:  1998

Review 2.  Genotype-phenotype correlations and differential diagnosis in autosomal dominant macular disease.

Authors:  A Iannaccone
Journal:  Doc Ophthalmol       Date:  2001-05       Impact factor: 2.379

3.  Colour vision as a diagnostic aid.

Authors:  A Pinckers
Journal:  Doc Ophthalmol       Date:  1982-01-29       Impact factor: 2.379

4.  Basic phenomena in acquired colour vision deficiency.

Authors:  A Pinckers; M Marré
Journal:  Doc Ophthalmol       Date:  1983-05-01       Impact factor: 2.379

5.  Retinal dystrophies associated with peripheral retinal vasculopathy.

Authors:  W S Grizzard; A F Deutman; A J Pinckers
Journal:  Br J Ophthalmol       Date:  1978-03       Impact factor: 4.638

  5 in total

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