Sneddon syndrome: A rare diagnosis

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...

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Bibliographic Details
Main Authors: D. Yu. Andriyashkina, A. A. Kondrashov, N. А. Shostak, N. A. Demidova, D. V. Yudin, D. Yu. Kulakov, G. R. Avetisian
Format: Article
Language:Russian
Published: IMA PRESS LLC 2022-12-01
Series:Научно-практическая ревматология
Subjects:
sneddon syndrome
recurrent strokes
acute cerebrovascular disease
livedo racemose
livedo reticularis
neuroectodermal syndrome
antiphospholipid syndrome
vasculopathy
anticoagulants
antiplatelets
Online Access:https://rsp.mediar-press.net/rsp/article/view/3255

Internet

https://rsp.mediar-press.net/rsp/article/view/3255

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