Literature DB >> 7411340

Retinal lesions in Alport's syndrome.

R Zylbermann, B Z Silverstone, E Brandes, A Drukker.   

Abstract

We described a family in which two siblings were suffering from Alport's syndrome. Both had identical ocular lesions: whitish-grey dots in the superficial layers of the retina mainly in the posterior pole. The visual acuity, the visual field, and the fundus fluorescein angiogram were normal. These lesions were associated with an impaired ERG. The ocular finding seems to be characteristic of the Alport's syndrome.

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Year:  1980        PMID: 7411340     DOI: 10.3928/0191-3913-19800701-15

Source DB:  PubMed          Journal:  J Pediatr Ophthalmol Strabismus        ISSN: 0191-3913            Impact factor:   1.402


  3 in total

Review 1.  Alport syndrome, basement membranes and collagen.

Authors:  C E Kashtan; M M Kleppel; R J Butkowski; A F Michael; A J Fish
Journal:  Pediatr Nephrol       Date:  1990-09       Impact factor: 3.714

2.  Ocular manifestations of Alport's syndrome: a hereditary disorder of basement membranes?

Authors:  J A Govan
Journal:  Br J Ophthalmol       Date:  1983-08       Impact factor: 4.638

3.  An electrophysiological study on children and young adults with Alport's syndrome.

Authors:  B G Jeffrey; M Jacobs; G Sa; T M Barratt; D Taylor; A Kriss
Journal:  Br J Ophthalmol       Date:  1994-01       Impact factor: 4.638

  3 in total

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