SICKLE CELL TRAIT, CLINICAL MANIFESTATIONS AND OUTCOMES: A CROSS-SECTIONAL STUDY

Introduction: Sickle cell trait (SCT) is an autosomal recessive blood disorder in which patients are heterozygous carriers for hemoglobin S (HbAS) and are usually asymptomatic. We performed a descriptive analysis of clinical manifestations and outcomes associated with SCT. Methods: This was a de...

全面介紹

書目詳細資料

Principais autores:	Diego A Vargas-Hernández, Adriana Catalina Uscategui-Ruiz, Andrés Jesus Prada-Rueda, Consuelo Romero-Sánchez
格式:	Artigo
語言:	Inglês
出版:	PAGEPress Publications 2023-02-01
叢編:	Mediterranean Journal of Hematology and Infectious Diseases
主題:	Sickle Cell Trait Splenic Infarction Splenic Diseases Spleen Hemoglobinopathies
在線閱讀:	http://www.mjhid.org/index.php/mjhid/article/view/5137
標簽:	添加標簽 沒有標簽, 成為第一個標記此記錄!