Results 181 to 190 of about 29,473,219 (216)
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Lin chuang er bi yan hou ke za zhi = Journal of clinical otorhinolaryngology, 2011
Neurofibromatosis type 2 (NF2) is an autosomal-dominant inherited tumour predisposition syndrome caused by mutations in the NF2 gene on chromosome 22. Affected individuals develop schwannomas characteristically affecting both vestibular nerves leading to hearing loss and eventual deafness.
Evans, GR; id_orcid 0000-0002-8482-5784 +2 more
+8 more sources
Neurofibromatosis type 2 (NF2) is an autosomal-dominant inherited tumour predisposition syndrome caused by mutations in the NF2 gene on chromosome 22. Affected individuals develop schwannomas characteristically affecting both vestibular nerves leading to hearing loss and eventual deafness.
Evans, GR; id_orcid 0000-0002-8482-5784 +2 more
+8 more sources
Zhonghua er bi yan hou ke za zhi, 2004
Type 2 neurofibromatosis (NF2) is an autosomal dominant disorder caused by mutations in the NF2 tumor suppressor gene NF2 on chromosome 22. Around 1 in 33000 people are born with an NF2 mutation although more than one-third of the 60% of de novo cases are not conceived with the mutation but this develops later in embryogenesis (mosaics).
D, Xie +7 more
openaire +4 more sources
Type 2 neurofibromatosis (NF2) is an autosomal dominant disorder caused by mutations in the NF2 tumor suppressor gene NF2 on chromosome 22. Around 1 in 33000 people are born with an NF2 mutation although more than one-third of the 60% of de novo cases are not conceived with the mutation but this develops later in embryogenesis (mosaics).
D, Xie +7 more
openaire +4 more sources
Acta Otorrinolaringológica Española, 2010
Type 2 neurofibromatosis (NF2) is an invalidating, inherited, dominant, autosomal disease. It is commonly confused with type 1 neurofibromatosis, although the two disorders are different. All subjects who inherit a mutated NF2 gene will develop the disease, which is characterised by the growth of schwannomas, generally affecting the vestibular nerve ...
Marta, Pérez-Grau +5 more
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Type 2 neurofibromatosis (NF2) is an invalidating, inherited, dominant, autosomal disease. It is commonly confused with type 1 neurofibromatosis, although the two disorders are different. All subjects who inherit a mutated NF2 gene will develop the disease, which is characterised by the growth of schwannomas, generally affecting the vestibular nerve ...
Marta, Pérez-Grau +5 more
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Otolaryngologic Clinics of North America, 2015
Neurofibromatosis type 2 (NF2) is a rare syndrome characterized by bilateral vestibular schwannomas, multiple meningiomas, cranial nerve tumors, spinal tumors, and eye abnormalities. NF2 presents unique challenges to the otologist because hearing loss may be the presenting complaint leading to the diagnosis of the disorder.
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Neurofibromatosis type 2 (NF2) is a rare syndrome characterized by bilateral vestibular schwannomas, multiple meningiomas, cranial nerve tumors, spinal tumors, and eye abnormalities. NF2 presents unique challenges to the otologist because hearing loss may be the presenting complaint leading to the diagnosis of the disorder.
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Pseudopapilledema in neurofibromatosis type 2
American Journal of Ophthalmology, 2000To report a case of neurofibromatosis type 2 with pseudopapilledema secondary to a prepapillary gliotic membrane.Case report. Results of an ocular examination and fluorescein angiography of a patient are described.Fundus examination of a 14-year-old male with neurofibromatosis type 2 revealed an irregular elevation of the optic nerve and a perifoveal ...
G T, Lueder, J T, Doll
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Neurofibromatosis Types 1 and 2
The Neurologist, 2006Neurofibromatosis types 1 and 2 (NF1 and NF2) are autosomal dominant neurocutaneous disorders with some similarities and many differences. They are frequently discussed together and often confused for one another by clinicians. Both disorders have widely variable presentations and degrees of severity. A thorough understanding of these complex disorders
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2013
Clinical History Image Findings Discussion Find Diagnosis Differential ...
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Clinical History Image Findings Discussion Find Diagnosis Differential ...
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Journal of the American Academy of Dermatology, 2001
K S, Caldemeyer, G W, Mirowski
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K S, Caldemeyer, G W, Mirowski
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2014
Clinical History: Patient presented with sudden unconsciousness. Patient had severe headache and decreased hearing since long time.
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Clinical History: Patient presented with sudden unconsciousness. Patient had severe headache and decreased hearing since long time.
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