Recurrent Hyperhemolysis Syndrome in Sickle Cell Disease

Sickle cell disease is a disorder of hemoglobin. The abnormal hemoglobin S disrupts blood flow, thereby resulting in acute painful sickle cell crisis. These episodes frequently prompt packed red blood cell transfusions to replace a patient’s functional hemoglobin stores. Production of alloantibodies...

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Detalles Bibliográficos
Autores principales: Rehman, Rafey, Saadat, Saad B, Tran, Deanna H, Constantinescu, Sinziana, Qamruzzaman, Yusuf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2021
Materias:
Hematology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195550/
https://www.ncbi.nlm.nih.gov/pubmed/34131536
http://dx.doi.org/10.7759/cureus.14991

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195550/
https://www.ncbi.nlm.nih.gov/pubmed/34131536
http://dx.doi.org/10.7759/cureus.14991

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