Stroke and presence of patent foramen ovale in sickle cell disease

Sickle cell disease (SCD) is an inherited monogenic hemoglobinopathy characterized by formation of sickle erythrocytes under conditions of deoxygenation. Sickle erythrocytes can lead to thrombus formation and vaso-occlusive episodes that may result in hemolytic anemia, pain crisis and multiple organ...

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Detalles Bibliográficos
Autores principales: Aggeli, Constantina, Polytarchou, Kali, Dimitroglou, Yannis, Patsourakos, Dimitrios, Delicou, Sophia, Vassilopoulou, Sophia, Tsiamis, Eleftherios, Tsioufis, Kostas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909731/
https://www.ncbi.nlm.nih.gov/pubmed/33638018
http://dx.doi.org/10.1007/s11239-021-02398-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7909731/
https://www.ncbi.nlm.nih.gov/pubmed/33638018
http://dx.doi.org/10.1007/s11239-021-02398-3

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