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CORRIGENDUM
Zdrav Vestn | May – June 2021 | Volume 90 | https://doi.org/10.6016/ZdravVestn.3282
eng slo element
en article-lang
10.6016/ZdravVestn.3282 doi
24.2.2021 date-received
31.5.2021 date-accepted
PODROČJEENG PODROČJE discipline
articletypeENG articletypeSLO article-type
Corrigendum // Clinical electrophysiological 
testing of the visual system: Review of the 
methods and indications for referral
Popravki avtorjev // Klinično elektrofiziološko 
testiranje vida: Pregled metod in indikacije za 
napotitev
article-title
Corrigendum Popravki avtorjev alt-title
KEYWORDS KLJUČNEBESEDE kwd-group
The authors declare that there are no conflicts 
of interest present.
Avtorji so izjavili, da ne obstajajo nobeni 
konkurenčni interesi. conflict
year volume first month last month first page last page
2021 90 5 6 360 360
name surname aff email
name surname aff
eng slo aff-id
Corrigendum
Corrigendum to: Šuštar M, Hawlina M, Brecelj J. Clinical electrophysiological testing 
of the visual system: Review of the methods and indications for referral. Zdrav Vestn. 
2020;89(7–8):378–97.
DOI: https://doi.org/10.6016/ZdravVestn.2975
Corrigendum: Zdrav Vestn. 2021;90(5–6):360–360. DOI: https://doi.org/10.6016/ZdravVestn.3282
Copyright (c) 2021 Slovenian Medical Journal. This work is licensed under a
Creative Commons Attribution-NonCommercial 4.0 International License.
In the original paper, references were accidentally omitted in Figure legend 
(Figure 4, Figure 8). These have now been corrected and list of references was 
updated.
Figure 4: Image of the fundus (A), image of fundus autofluorescence (B), optic 
coherent tomography (OCT) of the macula (C), and the results of electrophysiolo-
gical tests (D) for an 8-year-old girl with a genetically confirmed Stargardt disea-
se, also present in her older sister. Electrophysiological result has shown the impa-
irment of the rods and cones of the peripheral retinal function (abnormal DA and 
LA responses with ffERG), and the impairment of the macular function (abnormal 
mfERG), which was present already in the early phase, indicating a case of fast-pro-
gressing Stargardt disease (Figure adapted from Jarc Vidmar, 2012, 2015) (36,37).
Figure 8: The case of a patient with clinically atypical Leber hereditary optic neu-
ropathy. The results of electrophysiological tests on both eyes showed a normal flash 
ERG and a normal P50 of the pattern ERG, the N95 was raised above the baseline, 
VEP was not recordable (Figure adapted from Jarc Vidmar, 2019) (38).
References
36. Jarc Vidmar M, Perovšek D, Glavač D, Brecelj J, Hawlina M, Stirn Kranjc B. Morphology and function of the 
retina in children and young adults with Stargardt dystrophy. Zdrav Vestn. 2012;82(Suppl I):82.
37. Jarc-Vidmar M, Fakin A, Šuštar M, Brecelj J, Stirn-Kranjc B, Glavač D, Hawlina M. Interesting phenotype 
electrophysiological findings in a Slovene family with ABCA4 mutation. In: Hawlina M, Stirn-Kranjc B, eds. 
Programme and book of abstracts. Glasgow: International Society for Clinical Electrophysiology of Vision - 
ISCEV. Ljubljana: Slovenian Society of Ophthalmology; 2015. p. 78.
38. Jarc-Vidmar M, Kiraly P, Fakin A, Šuštar M, Volk M, Hawlina M. A Slovene family with LHON patients 
discovered after atypical presentation of LHON in a patient with occipital ischaemic stroke. Neuro-
ophthalmology. 2019; 43(Suppl. 1):83-84.