Multifocal Vitelliform Retinal Lesion
Authors:
T. Streicher 1; J. Špirková 1; M. Ilavská 2
Authors place of work:
Očné oddelenie NsP Bojnice, primárka MUDr. Ida Simonidesová
1; Očná ambulancia NsP sv. Lukáša Galanta, vedúca lekárka MUDr. Monika Ilavská, PhD
2
Published in the journal:
Čes. a slov. Oftal., 71, 2015, No. 3, p. 175-178
Category:
Case Report
Summary
The authors present retrospective follow up of patient with bilateral multifocal vitelliform retinal lesion during the 18 years period. At this time, spontaneous improvement of objective picture on retina and subjective visual troubles was observed. It is probable, that this case is a part of the same symptom complex as a variant of Best´s hereditary disease. This conclusion was based on initial stadium of phenotypical expressivity and additional evaluations. The course and outcomes of visual functions were different. The hereditary transmission was not confirmed.
Key words:
multifocal vitelliform retinal lesion, electrophysiology of retina, the fluorescence angiography, optical coherence tomography
Zdroje
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Štítky
OphthalmologyČlánok vyšiel v časopise
Czech and Slovak Ophthalmology
2015 Číslo 3
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