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Volume 24, Number 8—August 2018
Dispatch

Anncaliia algerae Microsporidial Myositis, New South Wales, Australia

Gaurav Sutrave, Adam Maundrell, Caitlin Keighley, Zoe Jennings, Susan Brammah, Min-Xia Wang, Roger Pamphlett, Cameron E. Webb, Damien Stark, Helen Englert, David Gottlieb, Ian Bilmon, and Matthew R. WattsComments to Author 
Author affiliations: Westmead Hospital, Westmead, New South Wales, Australia (G. Sutrave, A. Maundrell, C. Keighley, C.E. Webb, H. Englert, D. Gottlieb, I. Bilmon, M.R. Watts); University of Sydney, Sydney, New South Wales, Australia (G. Sutrave, M.-X. Wang, R. Pamphlett, C.E. Webb, D. Gottlieb, I. Bilmon, M.R. Watts); New South Wales Health Pathology Institute of Clinical Pathology and Medical Research, Westmead (Z. Jennings, C.E. Webb, M.R. Watts); Concord Repatriation General Hospital, Concord West, New South Wales, Australia (S. Brammah); St. Vincent’s Hospital, Darlinghurst, New South Wales, Australia (D. Stark)

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Table 1

Clinical features of 7 case-patients with Anncaliia algerae microsporidial myositis from North America and New South Wales, Australia*

Clinical feature
No. cases
Weakness 7
Muscle pain 7
Fever 6
Fatigue 6
Peripheral edema 6
Weight loss 5
Dysphagia 4
Glossitis 4
Diarrhea 4
Delirium 3
Congestive cardiac failure 1

*In 2 cases the clinical features were only sourced from published reports (1,5) rather than patient records (24).

Main Article

References
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Page updated: July 18, 2018
Page reviewed: July 18, 2018
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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