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Neurological Sciences
Published in: Neurological Sciences 6/2016

01-06-2016 | Letter to the Editor

Eye movement abnormalities in a patient with Zellweger spectrum disorder

Authors: F. Rosini, C. Vinciguerra, A. Mignarri, M. Di Giovanni, A. Federico, A. Rufa

Published in: Neurological Sciences | Issue 6/2016

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Excerpt

Dear Sir, …
Literature
1.
Mignarri A, Vinciguerra C, Giorgio A, Ferdinandusse S, Waterham H, Wanders R, Bertini E, Dotti MT, Federico A (2012) Zellweger spectrum disorder with mild phenotype caused by PEX2 gene mutations. JIMD Rep 6:43–46CrossRefPubMedPubMedCentral
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Noguer MT, Martinez M (2010) Visual follow-up in peroxisomal disorders patients treated with docosahexaenoic acid ethyl ester. Invest Ophthalmol Vis Sci 51(4):2277–2285CrossRefPubMed
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Kori AA, Robin NH, Jacobs JB, Erchul DM, Zaidat OO, Remler BF, Averbuch-Heller L, Dell’Osso LF, Leigh RJ, Zinn AB (1998) Pendular nystagmus in patients with peroxisomal assembly disorders. Arch Neurol 55:554–558CrossRefPubMed
4.
Leigh RJ, Zee DS (2015) The neurology of eye movements, 5th edn. Oxford University Press, New York
5.
Rosini F, Federighi P, Pretegiani E, Piu P, Leigh RJ, Serra A, Federico A, Rufa A (2013) Ocular-motor profile and effects of memantine in a familiar form of adult cerebellar ataxia with slow saccades and square wave saccadic intrusions. PLoS One 8:e69522CrossRefPubMedPubMedCentral
Metadata
Title
Eye movement abnormalities in a patient with Zellweger spectrum disorder
Authors
F. Rosini
C. Vinciguerra
A. Mignarri
M. Di Giovanni
A. Federico
A. Rufa
Publication date
01-06-2016
Publisher
Springer Milan
Published in
Neurological Sciences / Issue 6/2016
Print ISSN: 1590-1874
Electronic ISSN: 1590-3478
DOI
https://doi.org/10.1007/s10072-016-2499-8

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