Abstract
Wyburn-Mason’s syndrome is a rare neurocutaneous disorder characterised mainly by: (1) usually unilateral arteriovenous malformations of the (mid) brain; (2) vascular abnormalities of the retina, optic nerve, orbit, optic chiasm and tract; and (3) multiple cutaneous nevi consisting either of faint reddish-bluish discoloration or dilated enlarged superficial veins involving the trigeminal region (Younge 1987).
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Ruggieri, M., Konez, O., Rocco, C. (2008). Wyburn-Mason Syndrome. In: Ruggieri, M., Pascual-Castroviejo, I., Di Rocco, C. (eds) Neurocutaneous Disorders Phakomatoses and Hamartoneoplastic Syndromes. Springer, Vienna. https://doi.org/10.1007/978-3-211-69500-5_14
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DOI: https://doi.org/10.1007/978-3-211-69500-5_14
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