A case of facial-onset sensory and motor neuronopathy (FOSMN) with cerebellar ataxia and abnormal decrement in repetitive nerve stimulation test
Author:
Affiliation:
1. Department of Neurology, Sapporo Medical University School of Medicine
Publisher
Societas Neurologica Japonica
Subject
Clinical Neurology
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/61/2/61_cn-001508/_pdf
Reference25 articles.
1. 1) Vucic S, Tian D, Chong PS, et al. Facial onset sensory and motor neuronopathy (FOSMN syndrome): a novel syndrome in neurology. Brain 2006;129:3384-3390.
2. 2) Hokonohara T, Shigeto H, Kawano Y, et al. Facial onset sensory and motor neuronopathy (FOSMN) syndrome responding to immunotherapies. J Neurol Sci 2008;275: 157-158.
3. 3) Sonoda K, Sasaki K, Tateishi T, et al. TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: an autopsied case report and a review of the literature. J Neurol Sci 2013; 332:148-153.
4. 4) Ohashi N, Nonami J, Kodaira M, et al. Taste disorder in facial onset sensory and motor neuronopathy: a case report. BMC Neurol 2020;20:71.
5. 5) Fluchere F, Verschueren A, Cintas P, et al. Clinical features and follow-up of four new cases of facial-onset sensory and motor neuronopathy. Muscle Nerve 2011;43:136-140.
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