Fever in sickle cell disease patients in the Kingdom of Bahrain

• Egile Nagusiak: Jameela Al Salman (Egilea), Rawan A. Al Agha (Egilea), Safa Al Taitoon (Egilea), Amani Al Arrayed (Egilea)
• Formatua: Liburua
• Argitaratua: Elsevier, 2014-07-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Summary: Sickle cell disease (SCD) is a hereditary blood disorder characterized by abnormal red blood cell shape (sickling). The incidence of the disease in the Kingdom of Bahrain is approximately 2.1%. Patients with SCD are prone to multiple health complications, some of which are fatal. A retrospe...