MedPix COW 647 - Neurofibromatosis Type 2, the MISME Syndrome

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07/10/23

Neurofibromatosis type 2, contrary to it's name, is not associated with neurofibromas. Instea, NF2 is an autosomal dominant disease caused by a 22q mutation, associated with Multiple (lesions) due to an Inherited (mutation): Schwannoma, Meningioma, and Ependymoma (spinal). MedPix® Teaching Files - http://rad.usuhs.edu/medpix/pa....rent.php3?mode=tf2#t MedPix® is a Registered Trademark of USUHS

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