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...

Бүрэн тодорхойлолт

Номзүйн дэлгэрэнгүй

Үндсэн зохиолчид:	Diego A Vargas-Hernández, Adriana Catalina Uscategui-Ruiz, Andrés Jesus Prada-Rueda, Consuelo Romero-Sánchez
Формат:	Artigo
Хэл сонгох:	Inglês
Хэвлэсэн:	PAGEPress Publications 2023-02-01
Цуврал:	Mediterranean Journal of Hematology and Infectious Diseases
Нөхцлүүд:	Sickle Cell Trait Splenic Infarction Splenic Diseases Spleen Hemoglobinopathies
Онлайн хандалт:	http://www.mjhid.org/index.php/mjhid/article/view/5137
Шошгууд:	Шошго нэмэх Шошго байхгүй, Энэхүү баримтыг шошголох эхний хүн болох!