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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease neurofibromatosis 2
Comorbidity C0025286|meningioma
Sentences 4
PubMedID- 24778560 Mutations and/or deletions within the tumor suppressor gene neurofibromatosis type 2 (nf2) are associated with meningioma development and progression.
PubMedID- 24599662 Here, we describe an extremely rare case of angiosarcoma arising in schwannoma of the cerebellopontine angle and later associating with meningioma in a patient with neurofibromatosis type 2.
PubMedID- 25751482 Intractable yawning caused by foramen magnum meningioma in a patient with neurofibromatosis type 2.
PubMedID- 24448521 Purpose: the purpose of this study was to report a rare case of neurofibromatosis type 2 (nf2) with extracranial orbital meningioma extending into the frontal and ethmoidal sinuses.

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