Abstract
Wagner syndrome is a vitreoretinal degeneration, which is not associated with systemic features. The condition is characterised by mild myopia and an ‘optically empty’ vitreous (historically this caused confusion with Stickler syndrome) and is also associated with early-onset cortical cataract and progressive chorioretinal atrophy. The disorder is caused by mutation in the gene encoding versican (VCAN).
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Black, G.C.M. (2014). Wagner Syndrome. In: Puech, B., De Laey, JJ., Holder, G. (eds) Inherited Chorioretinal Dystrophies. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-69466-3_46
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DOI: https://doi.org/10.1007/978-3-540-69466-3_46
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