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Advancements in Sickle Cell Disease (SCD) Treatment: A Review of Novel Pharmacotherapies and Their Impact on Patient Outcomes

Sickle cell disease (SCD) is a genetic hereditary blood disease that disrupts normal beta-globin production. Patients with SCD experience a broad range of symptoms ranging from anemia, pain crises, and jaundice to acute coronary syndrome and stroke. SCD has been treated with hydroxyurea since 1998. ...

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Detalles Bibliográficos
Autores principales:	Khan, Salman J, Zaidi, Syed Asjad Tauheed, Murtaza, Syeda Fatima, Asif, Muhammad, Kumar, Vinod
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2023
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472971/ https://www.ncbi.nlm.nih.gov/pubmed/37664319 http://dx.doi.org/10.7759/cureus.42847

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