Neurofibromatosis 2 (NF2) is characterized by bilateral vestibular neurofibromas. Although the facial nerve, the cochlear nerve, and the superior division of the vestibular nerve can be evaluated before surgery, whether the inferior division of the vestibular nerve is affected remains undetermined without an operation. A total of 7 patients with NF2 (2 men and 5 women) underwent pure tone audiometry, caloric testing, vestibular evoked myogenic potential (VEMP ) testing, and magnetic resonance imaging. Audiometry revealed mean hearing levels of less than 26 dB for 1 ear, 26 to 70 dB for 8 ears, 71 to 90 dB for 3 ears, and more than 90 dB for 2 ears. Caloric testing revealed an absent response in 71% of the 14 ears. Seven ears underwent VEMP ...
Neurofibromatosis type II (NF II) is rare and most commonly presents with hearing loss, tinnitus and...
Neurofibromatosis type 2 (NF2) is an autosomal dominant inherited diseases. NF2 patients suffer a hi...
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized b...
Patients with neurofibromatosis type 2 (NF2) develop bilateral cochleovestibular schwannomas (CVSs) ...
Background: Neurofibromatosis Type 2 (NF2) is a dominantly inherited tumour syndrome with a phenotyp...
Neurofibromatosis type 2 (NF2) is an inherited disease which is mainly characterized by the developm...
Abstract Neurofibromatosis type 2 (NF2) is a tumour-prone disorder characterised by the development ...
Abstract Neurofibromatosis type 2 (NF2) is a rare genetic disease involving multiple tumors of the c...
AbstractIntroductionCervical vestibular evoked myogenic potentials (cVEMP) can assess the integrity ...
Copyright © 2012 Kiran Gangadhar et al. This is an open access article distributed under the Creativ...
A 27-year-old female presented with complaints of dizziness and tinnitus in the right ear. The neuro...
Abstract Introduction: Cervical vestibular evoked myogenic potentials (cVEMP) can assess the integr...
The radiological findings in six patients fulfilling the criteria of neurofibromatosis type 2 (NF2) ...
Introduction. Vestibular schwannomas (VS) are benign tumours of the vestibular nerve and can lead to...
A 5-year-old girl presented with multiple tumours of the central nervous system. As on the first MRI...
Neurofibromatosis type II (NF II) is rare and most commonly presents with hearing loss, tinnitus and...
Neurofibromatosis type 2 (NF2) is an autosomal dominant inherited diseases. NF2 patients suffer a hi...
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized b...
Patients with neurofibromatosis type 2 (NF2) develop bilateral cochleovestibular schwannomas (CVSs) ...
Background: Neurofibromatosis Type 2 (NF2) is a dominantly inherited tumour syndrome with a phenotyp...
Neurofibromatosis type 2 (NF2) is an inherited disease which is mainly characterized by the developm...
Abstract Neurofibromatosis type 2 (NF2) is a tumour-prone disorder characterised by the development ...
Abstract Neurofibromatosis type 2 (NF2) is a rare genetic disease involving multiple tumors of the c...
AbstractIntroductionCervical vestibular evoked myogenic potentials (cVEMP) can assess the integrity ...
Copyright © 2012 Kiran Gangadhar et al. This is an open access article distributed under the Creativ...
A 27-year-old female presented with complaints of dizziness and tinnitus in the right ear. The neuro...
Abstract Introduction: Cervical vestibular evoked myogenic potentials (cVEMP) can assess the integr...
The radiological findings in six patients fulfilling the criteria of neurofibromatosis type 2 (NF2) ...
Introduction. Vestibular schwannomas (VS) are benign tumours of the vestibular nerve and can lead to...
A 5-year-old girl presented with multiple tumours of the central nervous system. As on the first MRI...
Neurofibromatosis type II (NF II) is rare and most commonly presents with hearing loss, tinnitus and...
Neurofibromatosis type 2 (NF2) is an autosomal dominant inherited diseases. NF2 patients suffer a hi...
Neurofibromatosis 2 is a rare autosomal dominant neurocutaneous disorder classically characterized b...