Ophthalmological findings in children and adolescents with Silver-Russell syndromeShow others and affiliations
2011 (English)In: British Journal of Ophthalmology, ISSN 0007-1161, E-ISSN 1468-2079, Vol. 95, no 5, p. 637-641Article in journal (Refereed) Published
Abstract [en]
AIM: To evaluate ophthalmological findings in children with Silver-Russell syndrome (SRS).
METHODS: An ophthalmological evaluation including visual acuity (VA), refraction, strabismus, near point of convergence (NPC), slit-lamp examination, ophthalmoscopy, axial length measurements and full-field electroretinogram was performed on 18 children with SRS (8 girls, 10 boys; mean age 11.6 years). Fundus photographs were taken for digital image analysis. Data were compared with data on an age- and gender-matched reference group (ref) of school children (n=99).
RESULTS: Seventeen out of 18 children with SRS had ophthalmological abnormalities. Best corrected VA of the best eye was <0.1 log of the minimal angle of resolution in 11 children (ref n=98) (p<0.0001), and 11 children had refractive errors (ref n=33) (p=0.05). Anisometropia (≥1 dioptre) was noted in three of the children (ref n=3) (p=0.046). Subnormal stereo acuity and NPC were found in 2/16 (ref=0) (p=0.02). The total axial length in both eyes was shorter compared with that in controls (p<0.006 and p<0.001). Small optic discs were found in 3/16, large cup in 3/16 and increased tortuosity of retinal vessels in 4/13 children with SRS.
CONCLUSION: Children with SRS, who are severely intrauterine growth retarded, show significant ophthalmological abnormalities. Based on the present findings, ophthalmological examination is recommended in children with SRS.
Place, publisher, year, edition, pages
BMJ Publishing Group Ltd, 2011. Vol. 95, no 5, p. 637-641
National Category
Ophthalmology
Identifiers
URN: urn:nbn:se:oru:diva-103787DOI: 10.1136/bjo.2010.184457ISI: 000289717300011PubMedID: 20805133Scopus ID: 2-s2.0-79955023389OAI: oai:DiVA.org:oru-103787DiVA, id: diva2:1732028
Funder
Wilhelm och Martina Lundgrens VetenskapsfondSven Jerring FoundationSwedish Research Council, 10863
Note
Funding Agency:
Gothenburg Medical Society
2023-01-302023-01-302024-01-02Bibliographically approved