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Multiple respiratory complications in a patient with Charcot-Marie-Tooth disease with MFN2 mutation
Charcot-Marie-Tooth disease (CMT) is a hereditary peripheral neuropathy characterized by progressive atrophy of distal muscles. Respiratory complications are rare. We present a case of a 49-year-old male with childhood-onset CMT bearing a genetic mutation of MFN2. He had difficulty breathing when he...
Autores principales: | Sano, Tomoya, Miyata, Jun, Matsukida, Akira, Watanabe, Chie, Suematsu, Ryohei, Tagami, Yoichi, Kimizuka, Yoshifumi, Fujikura, Yuji, Kawana, Akihiko |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866735/ https://www.ncbi.nlm.nih.gov/pubmed/35242516 http://dx.doi.org/10.1016/j.rmcr.2022.101601 |
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