Sneddon syndrome: A rare diagnosis
| Autor: | D. Yu. Andriyashkina, A. A. Kondrashov, N. А. Shostak, N. A. Demidova, D. V. Yudin, D. Yu. Kulakov, G. R. Avetisian |
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| Jazyk: | ruština |
| Rok vydání: | 2022 |
| Předmět: | |
| Zdroj: | Научно-практическая ревматология, Vol 60, Iss 6, Pp 630-637 (2022) |
| Druh dokumentu: | article |
| ISSN: | 1995-4484 1995-4492 |
| DOI: | 10.47360/1995-4484-2022-630-637 |
| Popis: | The study objective is to demonstrate a rare cause of recurrent acute cerebrovascular diseases in a young patient – Sneddon syndrome. The patient revealed gene polymorphism: homozygous 4G/5G in the plasminogen activator inhibitor-1 (PAI-1) gene, C807T in the glycoprotein I gene (GPIa), T1565C in the glycoprotein III gene (GPIIIa), G1639A in the vitamin K epoxide reductase gene (VKORC1), increased homocysteine, which were risk factors for thrombosis. |
| Databáze: | Directory of Open Access Journals |
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