A case of Creutzfeldt-Jakob disease with E200K mutation presenting with hearing loss and central hypoventilation
Author:
Affiliation:
1. Department of Neurology, The Jikei University Kashiwa Hospital
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/58/11/58_cn-001197/_pdf
Reference9 articles.
1. 1) Orimo S, Ozawa E, Uematsu M, et al. A case of Creutzfeldt-Jakob disease presenting with auditory agnosia as an initial manifestation. Eur Neurol 2000;44:256-258.
2. 2) Salazar R, Cerghet M, Ramachandran V. Bilateral hearing loss heralding sporadic Creutzfeldt-Jakob disease: a case report and literature review. Otol Neurotol 2014;35:1327-1329.
3. 3) Rene R, Campdelacreu J, Ferrer I, et al. Familial Creutzfeldt-Jakob disease with E200K mutation presenting with neurosensorial hypoacusis. J Neurol Neurosurg Psychiatry 2007;78:103-104.
4. 4) Cataldi ML, Restivo O, Reggio E, et al. Deafness: an unusual onset of genetic Creutzfeldt-Jakob disease. Neurol Sci 2000;21:53-55.
5. 5) Atarashi R, Sano K, Satoh K, et al. Real-time quaking-induced conversion: a highly sensitive assay for prion detection. Prion 2011;5:150-153.
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1. Hearing impairment: an unexpected diagnosis;British Journal of Hospital Medicine;2020-12-02
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