Muscle carnitine deficiency: adult onset lipid storage myopathy with sensory neuropathy |
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Authors: | Wei Zhang Jianting Miao Guangyun Zhang Rui Liu Dawei Zhang Qun Wan Yingxin Yu Gang Zhao Zhuyi Li |
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Affiliation: | (1) Department of Neurology, Tangdu Hospital, Fourth Military Medical University, 710038 Xi’an, Shaanxi, China;(2) Department of Neurology, Xijing Hospital, Fourth Military Medical University, 710032 Xi’an, Shaanxi, China;(3) Department of Orthopaedics, Xijing Hospital, Fourth Military Medical University, 710032 Xi’an, Shaanxi, China; |
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Abstract: | Muscle carnitine deficiency usually results in a lipid storage myopathy, but more rarely, neuropathy occurs in this condition. We report herein a 29-year-old man with muscle carnitine deficiency who developed not only a lipid storage myopathy, but also a severe sensory neuropathy. Oral therapy with levo-carnitine (3 g per day) for 3 months produced a remarkable improvement of the myopathy and sensory neuropathy. Six months later, he remained in good condition under strict dietary control. This report emphasizes that severe neuropathy may occur in some patients with muscle carnitine deficiency, and highlights the need for the neurologist’s familiarity with those afflicted to achieve optimal clinical management. |
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