A framework for the evaluation of patients with congenital facial weakness
Abstract There is a broad differential for patients presenting with congenital facial weakness, and initial misdiagnosis unfortunately is common for this phenotypic presentation. Here we present a framework to guide evaluation of patients with congenital facial weakness disorders to enable accurate...
Main Authors: | Bryn D. Webb, Irini Manoli, Elizabeth C. Engle, Ethylin W. Jabs |
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Format: | Article |
Language: | English |
Published: |
BMC
2021-04-01
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Series: | Orphanet Journal of Rare Diseases |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13023-021-01736-1 |
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