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Neurofibromatosis 2 in children presenting during the first decade of life.

Cristina GaudiosoRobert ListernickMichael J FisherCynthia J CampenAlejandro PazDavid H Gutmann
Published in: Neurology (2019)
Although uncommon, a substantial number of individuals with NF2 come to medical attention in early childhood. The finding of meningioma or characteristic ocular abnormalities (retinal hamartomas and epiretinal membranes) in young children should raise clinical suspicion for NF2 and prompt immediate referral to appropriate specialists for diagnosis and management.
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