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Myofibrillar myopathy: a rare but important differential diagnosis of camptocormia in a patient with Parkinson’s Disease

Neurological Research and Practice
DOI: 10.1186/s42466-023-00250-y
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Abstract

Here we report on a patient with Parkinson's Disease and camptocormia due to Myofibrillar Myopathy Type 3. By leading the reader through the clinical reasoning process and highlighting the respective red flags we aim to increase the readers’ awareness for the differential diagnosis of camptocormia.

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Petry-Schmelzer, J. N., Abicht, A., Barbe, M. T., & Wunderlich, G. (2023, December 1). Myofibrillar myopathy: a rare but important differential diagnosis of camptocormia in a patient with Parkinson’s Disease. Neurological Research and Practice. BioMed Central Ltd. https://doi.org/10.1186/s42466-023-00250-y

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