File:FSHDDiagnosticTree.png

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Summary

Description
English: This is adapted from the information and diagram published by the American Academy of Neurology in 2015: Tawil, R; Kissel, JT; Heatwole, C; Pandya, S; Gronseth, G; Benatar, M; Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of, Neurology.; Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic, Medicine. (28 July 2015). "Evidence-based guideline summary: Evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine". Neurology. 85 (4): 357–64. doi:10.1212/WNL.0000000000001783. PMID 26215877.
Date
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Author Lukelahood

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Captions

American Academy of Neurology (ANN) guidelines for genetic testing for suspected FSHD. Not all laboratories follow this workflow.

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27 July 2021

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current01:22, 28 July 2021Thumbnail for version as of 01:22, 28 July 2021966 × 1,512 (159 KB)LukelahoodUploaded own work with UploadWizard
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