neurofibromatosis type ii การใช้

• "' Neurofibromatosis type II "'is a genetic condition which may be inherited or may arise spontaneously.
• Schwannomas can be associated with neurofibromatosis type II, which may be due to a loss-of-function mutation in the protein merlin.
• Neurofibromatosis type II ( NF-2 ) affects around 9 % of ONSM patients, where the incidence in the general population is around 0.03 0.05 %.
• The device, called the Nucleus 24 Multichannel Auditory Brainstem Implant, or ABI, is approved for use in teen-agers and adults with neurofibromatosis Type II, an inherited condition that affects about one American in 40, 000.