Camptocormia due to myotinilopathy, Parkinson's disease, or both? : Camptocormia and axial myopathy.
作者信息
Finsterer Josef
机构信息
Neurology & Neurophysiology Center, Postfach 20, 1180, Vienna, Austria.
出版信息
Neurol Res Pract. 2023 Sep 14;5(1):45. doi: 10.1186/s42466-023-00276-2.
Abstract
摘要
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Camptocormia due to myotinilopathy, Parkinson's disease, or both? : Camptocormia and axial myopathy.由肌强直病、帕金森病或两者共同导致的弯腰驼背：弯腰驼背与轴性肌病。
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Reply to: Camptocormia due to myotinilopathy, Parkinson's disease, or both?回复：弯腰驼背是由肌病、帕金森病还是两者共同引起的？
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Palmitoylethanolamide/Luteolin as Adjuvant Therapy to Improve an Unusual Case of Camptocormia in a Patient with Parkinson's Disease: A Case Report.棕榈酰乙醇胺/木犀草素作为辅助治疗改善帕金森病患者一例罕见的camptocormia病例：病例报告
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本文引用的文献
1
Myofibrillar myopathy: a rare but important differential diagnosis of camptocormia in a patient with Parkinson's Disease.肌原纤维肌病：帕金森病患者camptocormia的一种罕见但重要的鉴别诊断。
Neurol Res Pract. 2023 Jun 8;5(1):26. doi: 10.1186/s42466-023-00250-y.
2
Bi-Allelic Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function.导致影响骨骼肌和心脏功能的常染色体隐性肌原纤维肌病的双等位基因变异。
Int J Mol Sci. 2022 Dec 14;23(24):15906. doi: 10.3390/ijms232415906.
3
Clinical trajectory of a patient with filaminopathy who developed arrhythmogenic cardiomyopathy, myofibrillar myopathy, and multiorgan tumors.一名患有细丝蛋白病的患者的临床病程，该患者发展为致心律失常性心肌病、肌原纤维肌病和多器官肿瘤。
Neuromuscul Disord. 2021 Dec;31(12):1282-1286. doi: 10.1016/j.nmd.2021.10.002. Epub 2021 Oct 9.
4
Multisystem Myotilinopathy, including Myopathy and Left Ventricular Noncompaction, due to the Variant c.179C>T.多系统肌联蛋白病，包括肌病和左心室心肌致密化不全，由c.179C>T变异所致。
Case Rep Cardiol. 2020 May 13;2020:5128069. doi: 10.1155/2020/5128069. eCollection 2020.
5
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.由FLNC基因中的一个新型错义突变导致的具有异常组织病理学特征的肌原纤维肌病引起的心律失常和迟发性肌肉无力。
Rev Neurol (Paris). 2016 Oct;172(10):594-606. doi: 10.1016/j.neurol.2016.07.017. Epub 2016 Sep 12.
6
Camptocormia as presenting sign in myofibrillar myopathy.肌原纤维肌病以肌性斜颈为首发表现。
Neuromuscul Disord. 2012 Nov;22(11):987-9. doi: 10.1016/j.nmd.2012.06.004. Epub 2012 Jun 28.
7
Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q.与10号染色体长臂相关的常染色体显性遗传肌原纤维肌病伴致心律失常性右室心肌病
Ann Neurol. 1999 Nov;46(5):684-92. doi: 10.1002/1531-8249(199911)46:5<684::aid-ana2>3.0.co;2-#.
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