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A framework for the evaluation of patients with congenital facial weakness
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 diagnosis...
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| Publicat a: | Orphanet J Rare Dis |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2021
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8028830/ https://ncbi.nlm.nih.gov/pubmed/33827624 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-021-01736-1 |
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