Cargando…
Sexuality and sickle cell anemia
BACKGROUND: Sickle cell disease, the most common hereditary blood disease in the world, is the result of an atypical hemoglobin called S (Hb S) which, when homozygous (Hb SS) is the cause of sickle cell anemia. Changes of puberty, correlated with a delayed growth spurt, begin late in both male and f...
Autores principales: | Côbo, Viviane de Almeida, Chapadeiro, Cibele Alves, Ribeiro, João Batista, Moraes-Souza, Helio, Martins, Paulo Roberto Juliano |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Hematologia e
Hemoterapia
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3672116/ https://www.ncbi.nlm.nih.gov/pubmed/23741184 http://dx.doi.org/10.5581/1516-8484.20130027 |
Ejemplares similares
-
Rh E(w) antigen in a multi-transfused patient with sickle cell disease
por: Alves, Vitor Mendonça, et al.
Publicado: (2018) -
Cholelithiasis and its complications in sickle cell disease in a university hospital
por: Martins, Raquel Alves, et al.
Publicado: (2017) -
Haplotype of the β(S)-globin cluster in patients with sickle cell anemia at a University Hospital in the Triangulo Mineiro, Minas Gerais
por: Leal, Alexandra Silva, et al.
Publicado: (2015) -
Left ventricular hypertrophy in children, adolescents and young adults with sickle cell anemia
por: Faro, Gustavo Baptista de Almeida, et al.
Publicado: (2015) -
The influence of hydroxyurea on oxidative stress in sickle cell anemia
por: Torres, Lidiane de Souza, et al.
Publicado: (2012)