Sneddon syndrome: A rare diagnosis
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...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | Russian |
| Published: |
IMA PRESS LLC
2022-12-01
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| Series: | Научно-практическая ревматология |
| Subjects: | |
| Online Access: | https://rsp.mediar-press.net/rsp/article/view/3255 |
| _version_ | 1797862554438991872 |
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| author | D. Yu. Andriyashkina A. A. Kondrashov N. А. Shostak N. A. Demidova D. V. Yudin D. Yu. Kulakov G. R. Avetisian |
| author_facet | D. Yu. Andriyashkina A. A. Kondrashov N. А. Shostak N. A. Demidova D. V. Yudin D. Yu. Kulakov G. R. Avetisian |
| author_sort | D. Yu. Andriyashkina |
| collection | DOAJ |
| description | 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. |
| first_indexed | 2024-04-09T22:22:20Z |
| format | Article |
| id | doaj.art-fc8a7b1a75f84c0ab643dab23da31725 |
| institution | Directory Open Access Journal |
| issn | 1995-4484 1995-4492 |
| language | Russian |
| last_indexed | 2024-04-09T22:22:20Z |
| publishDate | 2022-12-01 |
| publisher | IMA PRESS LLC |
| record_format | Article |
| series | Научно-практическая ревматология |
| spelling | doaj.art-fc8a7b1a75f84c0ab643dab23da317252023-03-22T13:45:58ZrusIMA PRESS LLCНаучно-практическая ревматология1995-44841995-44922022-12-0160663063710.47360/1995-4484-2022-630-6372867Sneddon syndrome: A rare diagnosisD. Yu. Andriyashkina0A. A. Kondrashov1N. А. Shostak2N. A. Demidova3D. V. Yudin4D. Yu. Kulakov5G. R. Avetisian6N.I. Pirogov Russian National Research Medical UniversityN.I. Pirogov Russian National Research Medical UniversityN.I. Pirogov Russian National Research Medical UniversityN.I. Pirogov Russian National Research Medical UniversityN.I. Pirogov Russian National Research Medical UniversityN.I. Pirogov Russian National Research Medical UniversityN.I. Pirogov Russian National Research Medical UniversityThe 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.https://rsp.mediar-press.net/rsp/article/view/3255sneddon syndromerecurrent strokesacute cerebrovascular diseaselivedo racemoselivedo reticularisneuroectodermal syndromeantiphospholipid syndromevasculopathyanticoagulantsantiplatelets |
| spellingShingle | D. Yu. Andriyashkina A. A. Kondrashov N. А. Shostak N. A. Demidova D. V. Yudin D. Yu. Kulakov G. R. Avetisian Sneddon syndrome: A rare diagnosis Научно-практическая ревматология sneddon syndrome recurrent strokes acute cerebrovascular disease livedo racemose livedo reticularis neuroectodermal syndrome antiphospholipid syndrome vasculopathy anticoagulants antiplatelets |
| title | Sneddon syndrome: A rare diagnosis |
| title_full | Sneddon syndrome: A rare diagnosis |
| title_fullStr | Sneddon syndrome: A rare diagnosis |
| title_full_unstemmed | Sneddon syndrome: A rare diagnosis |
| title_short | Sneddon syndrome: A rare diagnosis |
| title_sort | sneddon syndrome a rare diagnosis |
| topic | sneddon syndrome recurrent strokes acute cerebrovascular disease livedo racemose livedo reticularis neuroectodermal syndrome antiphospholipid syndrome vasculopathy anticoagulants antiplatelets |
| url | https://rsp.mediar-press.net/rsp/article/view/3255 |
| work_keys_str_mv | AT dyuandriyashkina sneddonsyndromeararediagnosis AT aakondrashov sneddonsyndromeararediagnosis AT nashostak sneddonsyndromeararediagnosis AT nademidova sneddonsyndromeararediagnosis AT dvyudin sneddonsyndromeararediagnosis AT dyukulakov sneddonsyndromeararediagnosis AT gravetisian sneddonsyndromeararediagnosis |