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［1］ Patzko A, Shy ME. Charcot-Marie-Tooth disease and related genetic neuropathies. Continuum (Minneap-Minn), 2012, 18 (1): 39-59.
［2］ Tazir M, Hamadouche T, Nouioua S, et al. Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update. J Neurol Sci, 2014, 347 (1-2): 14-22.
［3］ Yiu EM, Brockley CR, Lee KJ, et al. Peripheral nerve ultrasound in pediatric Charcot-Marie-Tooth disease type 1A. Neurology, 2015, 84 (6): 569-574.
［4］ Hoyle JC, Isfort MC, Roggenbuck J, et al. The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and management. Appl Clin Genet, 2015, 8: 235-243.
［5］ Manganelli F, Nolano M, Pisciotta C, et al. Charcot-Marie-Tooth disease: New insights from skin biopsy. Neurology, 2015, 85 (14): 1202-1208.
［6］ Corrado B, Ciardi G, Bargigli C. Rehabilitation Management of the Charcot-Marie-Tooth Syndrome: A Systematic Review of the Literature. Medicine (Baltimore), 2016, 95 (17): e3278.
［7］ 徐银燕，张江涛，牛婧雯，等.进行性四肢麻木无力4年.中国现代神经疾病杂志，2017，017，17 (1):74-77.