Camptocormia due to myotinilopathy, Parkinson’s disease, or both?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1186/s42466-023-00276-2.pdf
Reference8 articles.
1. Petry-Schmelzer, J. N., Abicht, A., Barbe, M. T., & Wunderlich, G. (2023). Myofibrillar myopathy: A rare but important differential diagnosis of camptocormia in a patient with Parkinson’s Disease. Neurol Res Pract, 5(1), 26. https://doi.org/10.1186/s42466-023-00250-y.
2. Melberg, A., Oldfors, A., Blomström-Lundqvist, C., Stålberg, E., Carlsson, B., Larrson, E., Lidell, C., Eeg-Olofsson, K. E., Wikström, G., Henriksson, G., & Dahl, N. (1999). Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q. Annals Of Neurology, 46(5), 684–692. https://doi.org/10.1002/1531-8249(199911)46:5<684::aid-ana2>3.0.co;2-#.
3. Renard, D., Castelnovo, G., Fernandez, C., De Paula, A. M., Penttilä, S., Suominen, T., & Udd, B. (2012). Camptocormia as presenting sign in myofibrillar myopathy. Neuromuscular Disorders, 22(11), 987–989. https://doi.org/10.1016/j.nmd.2012.06.004.
4. Pongmala, C., Artusi, C. A., Zibetti, M., Pitakpatapee, Y., Wangthumrong, T., Sangpeamsook, T., Srikajon, J., Srivanitchapoom, P., Youn, J., Cho, J. W., Kim, M., Zamil Shinawi, H. M., Obaid, M. T., Baumann, A., Margraf, N. G., Pona-Ferreira, F., Leitão, M., Lobo, T., Ferreira, J. J., Fabbri, M., & Lopiano, L. (2022). Postural abnormalities in asian and caucasian Parkinson’s disease patients: A multicenter study. Parkinsonism & Related Disorders, 97, 91–98. https://doi.org/10.1016/j.parkreldis.2022.03.006.
5. Finsterer, J., Stöllberger, C., Hasun, M., Riedhammer, K., & Wagner, M. (2020). Multisystem myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the MYOT variant c.179 C > T. Case Rep Cardiol, 2020, 5128069. https://doi.org/10.1155/2020/5128069.
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