TY - JOUR
T1 - THE TARGET SIGN
T2 - A Near Infrared Feature and Multimodal Imaging in a Pluri-Ethnic Cohort with RDH5 -Related Fundus Albipunctatus
AU - Newman, Hadas
AU - Perlman, Ido
AU - Pras, Eran
AU - Rozenberg, Assaf
AU - Ben-Yosef, Tamar
AU - Iovino, Claudio
AU - Simonelli, Francesca
AU - Di Iorio, Valentina
AU - Rotenstreich, Ygal
AU - Katzburg, Etti
AU - Ehrenberg, Miriam
AU - Iglicki, Matias
AU - Zur, Dinah
N1 - Publisher Copyright:
© 2022 Lippincott Williams and Wilkins. All rights reserved.
PY - 2022/7/1
Y1 - 2022/7/1
N2 - Purpose:Retinol dehydrogenase 5 (RDH5)-related fundus albipunctatus can present with phenotypic variability. Our purpose was to investigate new clinical characteristics and multimodal imaging findings in patients from different ethnic origins, carrying different mutations.Methods:Multicenter international retrospective case series of 18 patients with genetically confirmed RDH5-related fundus albipunctatus. Patients' files were reviewed for fundus images, visual acuity, macular optical coherence tomography scans, near-infrared images, fundus autofluorescence, electroretinogram, and genetic mutations. Imaging and electroretinogram findings.Results:All eyes (n = 36, 100%) showed small circular findings seen on near-infrared images, termed as the "target sign," correlating to the yellowish dots seen clinically and to the distinct hyperreflective linear lesions on optical coherence tomography at the level between external limiting membrane and retinal pigment epithelium. Perifoveal atrophy with foveal sparing was seen in 4 eyes of 2 patients (both RDH5 - c.160C>T, p.R54X mutation). Fundus autofluorescence revealed small hyperautofluorescent dots (n = 16, 44.4%). Scotopic electroretinograms were significantly reduced in all cases with an electronegative pattern, 66.7% displayed cone dysfunction.Conclusion:Our results show distinct imaging findings present in all patients with fundus albipunctatus independent of ethnicity or genetic mutation. Our results can facilitate the current algorithm to diagnose RDH5-related fundus albipunctatus and allow for targeted genetic testing.
AB - Purpose:Retinol dehydrogenase 5 (RDH5)-related fundus albipunctatus can present with phenotypic variability. Our purpose was to investigate new clinical characteristics and multimodal imaging findings in patients from different ethnic origins, carrying different mutations.Methods:Multicenter international retrospective case series of 18 patients with genetically confirmed RDH5-related fundus albipunctatus. Patients' files were reviewed for fundus images, visual acuity, macular optical coherence tomography scans, near-infrared images, fundus autofluorescence, electroretinogram, and genetic mutations. Imaging and electroretinogram findings.Results:All eyes (n = 36, 100%) showed small circular findings seen on near-infrared images, termed as the "target sign," correlating to the yellowish dots seen clinically and to the distinct hyperreflective linear lesions on optical coherence tomography at the level between external limiting membrane and retinal pigment epithelium. Perifoveal atrophy with foveal sparing was seen in 4 eyes of 2 patients (both RDH5 - c.160C>T, p.R54X mutation). Fundus autofluorescence revealed small hyperautofluorescent dots (n = 16, 44.4%). Scotopic electroretinograms were significantly reduced in all cases with an electronegative pattern, 66.7% displayed cone dysfunction.Conclusion:Our results show distinct imaging findings present in all patients with fundus albipunctatus independent of ethnicity or genetic mutation. Our results can facilitate the current algorithm to diagnose RDH5-related fundus albipunctatus and allow for targeted genetic testing.
KW - Alcohol Oxidoreductases
KW - Electroretinography
KW - Ethnicity
KW - Fluorescein Angiography
KW - Humans
KW - Multimodal Imaging
KW - Night Blindness/diagnosis
KW - Retinal Diseases
KW - Retinal Dystrophies
KW - Retrospective Studies
KW - Tomography, Optical Coherence
KW - inherited retinal diseases
KW - multimodal imaging
KW - RDH5
KW - night blindness
KW - fundus albipunctatus
UR - http://www.scopus.com/inward/record.url?scp=85132454950&partnerID=8YFLogxK
U2 - 10.1097/iae.0000000000003466
DO - 10.1097/iae.0000000000003466
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C2 - 35250012
AN - SCOPUS:85132454950
SN - 0275-004X
VL - 42
SP - 1364
EP - 1369
JO - Retina
JF - Retina
IS - 7
ER -