Neurofibromatosis 2 D016518

Related MeSH Hierarchy (12)

Diseases [C] » Neoplasms [C04] » Neoplastic Syndromes, Hereditary » Neurofibromatoses » Neurofibromatosis 2

Diseases [C] » Otorhinolaryngologic Diseases [C09] » Otorhinolaryngologic Neoplasms » Neuroma, Acoustic » Neurofibromatosis 2

Diseases [C] » Nervous System Diseases [C10] » Cranial Nerve Diseases » Cranial Nerve Neoplasms » Neuroma, Acoustic » Neurofibromatosis 2

Diseases [C] » Nervous System Diseases [C10] » Neurocutaneous Syndromes » Neurofibromatoses » Neurofibromatosis 2

Description

An autosomal dominant disorder characterized by a high incidence of bilateral acoustic neuromas as well as schwannomas (NEURILEMMOMA) of other cranial and peripheral nerves, and other benign intracranial tumors including meningiomas, ependymomas, spinal neurofibromas, and gliomas. The disease has been linked to mutations of the NF2 gene (GENES, NEUROFIBROMATOSIS 2) on chromosome 22 (22q12) and usually presents clinically in the first or second decade of life.   MeSH


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