An 18-year-old man of hereditary neuropathy with liability to pressure palsies presenting with bilateral brachial plexopathy during military training
Author:
Affiliation:
1. Department of Clinical Neuroscience and Neurology, Yamaguchi University Graduate School of Medicine
2. Department of Neurology, Graduate School of Medicine, Nippon Medical School
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/61/10/61_cn-001619/_pdf
Reference12 articles.
1. 1) Lupski JR, Chance PF. Hereditary motor and sensory neuropathies involving altered dosage or mutation of PMP22: the CMT1A duplication and HNPP deletion. Dyck PJ, Thomas PK, editors. In: Peripheral Neuropathy. Fourth edition. Philadelphia: Elsevier Saunders; 2005. p. 1659-1680.
2. 2) Chance PF. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy. Neuromolecular Med 2006;8:159-174.
3. 3) 岩堀祐介，辻野昭人．肩関節周辺神経障害の病態と治療．MB Med Reha 2013;157:163-179.
4. 4) 中野隆．胸郭出口症候群の理解に必要な腕神経叢の解剖．整形・災害外科 2019;62:111-118.
5. 5) 園生雅弘，安藤哲明，内堀歩ら．True neurogenic thoracic outlet syndrome（TOS）の臨床的・電気生理学的特徴．臨床神経生理学 2012;40:131-139.
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