Leg Ulcers in Sickle Cell Disease: A Multifactorial Analysis Highlights the Hemolytic Profile

Sickle cell disease (SCD) is characterized by the presence of the variant S hemoglobin (HbS). The homozygous genotype (HbSS) is sickle cell anemia (SCA), while the double heterozygous of HbS and HbC (HbSC) is defined as SC hemoglobinopathy. The pathophysiology is based on chronic hemolysis, inflamma...

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Detalles Bibliográficos
Autores principales: Santos, Edvan do Carmo, Santana, Paulo Vinícius Bispo, de Jesus, Laíne Lopes Silva, Melo, Gabriela Imbassahy Valentim, Yahouédéhou, Sètondji Cocou Modeste Alexandre, da Guarda, Caroline Conceição, Santiago, Rayra Pereira, Fiuza, Luciana Magalhães, Carvalho, Suéllen Pinheiro, dos Santos, Liz Oliveira, Adorno, Elisângela Vitória, Aleluia, Augusto Cezar Magalhães, Luiz, Luciene Cristina Gastalho Campos, Fonseca, Teresa Cristina Cardoso, Gonçalves, Marilda de Souza, Aleluia, Milena Magalhães
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945128/
https://www.ncbi.nlm.nih.gov/pubmed/36810556
http://dx.doi.org/10.3390/hematolrep15010013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945128/
https://www.ncbi.nlm.nih.gov/pubmed/36810556
http://dx.doi.org/10.3390/hematolrep15010013

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