[HTML][HTML] Pathophysiologic basis of haemolysis in patients with sickle cell disease in steady state and in hyperhaemolytic states: aetiopathogenesis, management, and …
SG Ahmed, UA Ibrahim - Nigerian Journal of Basic and Clinical …, 2023 - journals.lww.com
Sickle cell disease (SCD) is characterized by red cell sickling, tissue infarcts, pain and
haemolysis. Haemolysis leads to anaemia, transfusion and vasculopathic multi-organ …
haemolysis. Haemolysis leads to anaemia, transfusion and vasculopathic multi-organ …
[HTML][HTML] Sonographic Assessment of Splenic Manifestations in Sickle Cell Disease Patients and Its Relation to Hematological Parameters: A Cross-Sectional Study in …
HS Sadeq, AS Abdulkareem, QM Dawood… - Cureus, 2024 - pmc.ncbi.nlm.nih.gov
Background Hemoglobinopathies, such as sickle cell disease (SCD), are inherited disorders
of hemoglobin (Hb) synthesis. SCD presents with complex clinical manifestations, including …
of hemoglobin (Hb) synthesis. SCD presents with complex clinical manifestations, including …
The role of acute and chronic splenic dysfunctions in aetiopathogenesis of anaemia in sickle cell disease: narrative review of hyperhaemolytic implications of …
SG Ahmed, UA Ibrahim - Nigerian Health Journal, 2023 - ajol.info
Background: Splenic dysfunction (SD) in SCD occurs due to one of two 'diametrically
opposed'anatomical manifestations: splenomegaly or autosplenectomy. Literature on SD …
opposed'anatomical manifestations: splenomegaly or autosplenectomy. Literature on SD …
[引用][C] Prevalence and clinical correlates of splenomegaly in sickle cell disease patients: An observational study in Western India
U Yanamandra, A Mahajan, G Jalal… - Medical Journal Armed …, 2024 - Elsevier