Sebastian syndrome (Q96602): Difference between revisions
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15 August 2026
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Latest revision as of 12:37, 16 August 2026
Sebastian syndrome is one of the MYH9 syndromes (a group that includes four clinical forms with similar manifestations resulting from mutations in the MYH9 gene: May-Hegglin anomaly and Fechtner and Epstein syndromes), which are characterised by a macrothrombocytopenia that is usually severe but paradoxically results in few if any symptoms.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1578628103 |
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| English | Sebastian syndrome |
Sebastian syndrome is one of the MYH9 syndromes (a group that includes four clinical forms with similar manifestations resulting from mutations in the MYH9 gene: May-Hegglin anomaly and Fechtner and Epstein syndromes), which are characterised by a macrothrombocytopenia that is usually severe but paradoxically results in few if any symptoms. |
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CID11:ID_1578628103
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dki-india-ID_1578628103
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Concluído
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15 August 2026
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