MedPix COW 647 - Neurofibromatosis Type 2, the MISME Syndrome

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)

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