Sonographic Assessment of Splenic Manifestations in Sickle Cell Disease Patients and Its Relation to Hematological Parameters: A Cross-Sectional Study in Basra, Iraq

Background Hemoglobinopathies, such as sickle cell disease (SCD), are inherited disorders of hemoglobin (Hb) synthesis. SCD presents with complex clinical manifestations, including anemia, painful episodes, and organ damage due to recurrent vaso-occlusion. The spleen is one of the first organs affec...

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Veröffentlicht in:	Curēus (Palo Alto, CA) CA), 2024-10, Vol.16 (10), p.e72322
Hauptverfasser:	Sadeq, Hussein S, Abdulkareem, Amenah S, Dawood, Qutaiba M, Khalaf, Asaad A
Format:	Artikel
Sprache:	eng
Schlagworte:	Age Anemia Blood Blood diseases Confidentiality Cross-sectional studies Data collection Demographics Hematology Hemoglobin Ischemia Mutation Outpatient care facilities Patients Questionnaires Radiology Sickle cell disease Spleen Statistical analysis Ultrasonic imaging Variance analysis
Online-Zugang:	Volltext
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