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Hereditary angioedema: the challenges of cross-border family investigation and treatment
Hereditary angioedema (HAE) is a rare genetic disorder characterised by recurrent swellings involving subcutaneous and submucosal tissue that can be potentially life threatening in cases involving the upper airway. In this case report, we present a Syrian refugee family with HAE who have lived in De...
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| Udgivet i: | BMJ Case Rep |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMJ Publishing Group
2020
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7199096/ https://ncbi.nlm.nih.gov/pubmed/32295794 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2019-231906 |
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