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Visual function, ocular motility and ocular characteristics in patients with mitochondrial complex I deficiency
Karolinska Institutet.
Karolinska Institutet.
Karolinska Institutet.
Karolinska University Hospital.
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2012 (English)In: Acta ophthalmologica, ISSN 1755-3768, Vol. 90, no 1, p. 32-43Article in journal (Refereed) Published
Abstract [en]

Abstract. Purpose: The aims of the present study were to investigate visual function, ocular motility and ocular characteristics in children and young adults with complex I deficiency. Material and Methods: In a prospective study with longitudinal follow-up, the visual and ocular outcome in 13 patients with deficiency in complex I [nicotine-amide adenine dinucleotide (NADH) dehydrogenase] in the mitochondrial respiratory chain is presented. The patients were diagnosed during 1995-2007 and assessed during 1997-2009 at a median age of 12.8 years (range 3.1-23.4). Results: Twelve of 13 patients had visual impairment and/or ocular pathology. Four of 10 patients who co-operated in visual assessment had a best corrected decimal visual acuity of A mutation in mitochondrial DNA. Only one patient had normal visual acuity and ocular outcome including refraction and visual fields. Follow-up time was median 3.0 years (range 0-11). Conclusion: Visual impairment, ocular motility problems and OA are common in children and young adults with complex I deficiency and should prompt the paediatric ophthalmologist to consider mitochondrial disorders.

Place, publisher, year, edition, pages
2012. Vol. 90, no 1, p. 32-43
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Health Sciences
Identifiers
URN: urn:nbn:se:mdh:diva-10564DOI: 10.1111/j.1755-3768.2010.01865.xISI: 000299624600028PubMedID: 20346082OAI: oai:DiVA.org:mdh-10564DiVA, id: diva2:360158
Available from: 2010-11-02 Created: 2010-10-27 Last updated: 2017-09-27Bibliographically approved

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  • apa
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