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The May-Hegglin anomaly: a rare cause of a common complaint
May-Hegglin anomaly is the presentation of a qualitative platelet disorder characterised by large platelets, thrombocytopenia and granulocyte inclusions as a result of mutations in the MYH9 gene. Though often overlooked given its rarity, it should be considered in patients who present with epistaxis...
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| Published in: | BMJ Case Rep |
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| Main Authors: | , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
BMJ Publishing Group
2021
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7929858/ https://ncbi.nlm.nih.gov/pubmed/33649034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2020-235432 |
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