神経線維腫症2型
1. Neurofibromatosis type IINeurofibromatosis Type II is an inherited disease. The main manifestation of the disease is the development of symmetric, non-malignant brain tumors in the region of the cranial nerve VIII, which is the auditory-vestibular nerve that transmits sensory information from the inner ear to the brain. Most people with this condition also experience problems in their eyes. NF II is caused by mutations of the "Merlin" gene, which, it seems, influences the form and movement of cells.
Read “Neurofibromatosis type II” on English Wikipedia
Read “神経線維腫症2型” on Japanese Wikipedia
Read “Neurofibromatosis type II” on DBpedia
Read “Neurofibromatosis type II” on English Wikipedia
Read “神経線維腫症2型” on Japanese Wikipedia
Read “Neurofibromatosis type II” on DBpedia
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