Dursun syndrome (Q107334): Difference between revisions
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A síndrome de Dursun é um transtorno genético caracterizado por hipertensão arterial pulmonar familiar, anormalidades cardíacas, incluindo defeito do septo atrial, leucopenia incluindo neutropenia intermitente, linfopenia, monocitose e anemia. | |||
| description / en | description / en | ||
Dursun syndrome is a genetic disorder characterised by familial pulmonary arterial hypertension, cardiac abnormalities including atrial septal defect, leukopenia including intermittent neutropaenia, lymphopenia, monocytosis, and anaemia. | |||
Revision as of 14:19, 17 August 2026
Dursun syndrome is a genetic disorder characterised by familial pulmonary arterial hypertension, cardiac abnormalities including atrial septal defect, leukopenia including intermittent neutropaenia, lymphopenia, monocytosis, and anaemia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_232201917 |
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| English | Dursun syndrome |
Dursun syndrome is a genetic disorder characterised by familial pulmonary arterial hypertension, cardiac abnormalities including atrial septal defect, leukopenia including intermittent neutropaenia, lymphopenia, monocytosis, and anaemia. |
