Sebastian syndrome (Q96602): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Verification Status | |||
Concluído | |||
| Property / Verification Status: Concluído / rank | |||
Normal rank | |||
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 |
||
| 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. |
Statements
CID11:ID_1578628103
0 references
dki-india-ID_1578628103
0 references
Concluído
0 references
