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...
- 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)