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[Treatment of Goldmann-Favre syndrome with cyclosporin A and bromocriptine].

Abstract
Up to now several reports have described a disturbance of humoral and cellular immune response in patients with tapetoretinal degeneration, but a pathogenetic relation of the described immunological changes to the retinal disease was not established. Therefore immunosuppressive treatment has not been advocated for degenerative vitreoretinal disease. We now report about the natural course of Goldmann-Favre's vitreo-retinal degeneration and the results of a therapeutical trial with cyclosporin A and bromocriptine in two patients. Without therapy we saw a slowly progressive flat central retinoschisis with a serous macular exsudation in fluorescein-angiography. Additionally we found peripheral vitreoretinal changes, mild cellular vitreal infiltration, extinguished electro-retinogram and disturbed dark adaptation. Visual acuity and visual field were quite stabile. Under therapy with cyclosporin A we found a regression of the macular edema and flattening of the retinoschisis. One of the two cases showed a good improvement of visual acuity, in the other case a clear subjective improvement did not correlate with an increase in visual acuity. An additional therapy with bromocriptine did not bring further success, but we were able to reduce the cyclosporin A to a blood concentration of 70-100 ng per ml.
AuthorsJ Garweg, M Böhnke, I Mangold
JournalKlinische Monatsblatter fur Augenheilkunde (Klin Monbl Augenheilkd) Vol. 199 Issue 3 Pg. 199-205 (Sep 1991) ISSN: 0023-2165 [Print] Germany
Vernacular TitleDie Behandlung des Goldmann-Favre-Syndroms mit Cyclosporin A und Bromocriptin.
PMID1753674 (Publication Type: Case Reports, English Abstract, Journal Article)
Chemical References
  • Bromocriptine
  • Cyclosporine
  • Prednisone
Topics
  • Adult
  • Bromocriptine (therapeutic use)
  • Cyclosporine (therapeutic use)
  • Diseases in Twins (genetics)
  • Drug Therapy, Combination
  • Female
  • Fluorescein Angiography
  • Genes, Recessive (genetics)
  • Humans
  • Prednisone (therapeutic use)
  • Retinitis Pigmentosa (drug therapy, genetics)
  • Syndrome
  • Visual Acuity (drug effects)

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