Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC)

Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present highly variable clinical manifestations. Sickle cell anemia (SCA) is the most severe form, while SC hemoglobinopathy (HbSC) is thought to be milder. Thus, we investigated the clinical manifestations and...

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Bibliografski detalji
Izdano u:PLoS One
Glavni autori: da Guarda, Caroline Conceição, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Santiago, Rayra Pereira, Neres, Joelma Santana dos Santos, Fernandes, Camila Felix de Lima, Aleluia, Milena Magalhães, Figueiredo, Camylla Vilas Boas, Fiuza, Luciana Magalhães, Carvalho, Suellen Pinheiro, de Oliveira, Rodrigo Mota, Fonseca, Cleverson Alves, Ndidi, Uche Samuel, Nascimento, Valma Maria Lopes, Rocha, Larissa Carneiro, Goncalves, Marilda Souza
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2020
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6988974/
https://ncbi.nlm.nih.gov/pubmed/31995624
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0228399
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