Sickle cell disease: A diagnosis to keep in mind

Sickle cell disease (SCD) is an autosomal recessive genetic disorder. It is the most frequent structural hemoglobinopathy worldwide, and it is produced by an alteration in the globin chain genes. In Chile, there is no data on the prevalence of SCD since it is considered a very rare condition. The in...

Full description

Autores:
Tipo de recurso:
Fecha de publicación:
2018
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22967
Acceso en línea:
https://doi.org/10.4067/S0370-41062018005000604
https://repository.urosario.edu.co/handle/10336/22967
Palabra clave:
Anemia
Hemoglobinopathy
Morbidity
Pathophysiology
Prevalence
Review
Sickle cell anemia
Differential diagnosis
Human
Multimodality cancer therapy
Prognosis
Sickle cell anemia
Combined modality therapy
Humans
Prognosis
Anemia
Hemoglobin
Hemoglobinopathies
Sickle cell
sickle cell
differential
Anemia
Diagnosis
Rights
License
Abierto (Texto Completo)