RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Engelhardt, Thomas SR Print(0) ID 1164085216 T1 Sickle Cell Disease (SCD) T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e YR 2019 FD 2019 PB McGraw-Hill Education PP New York, NY SN 9781259861789 LK accesspediatrics.mhmedical.com/content.aspx?aid=1164085216 RD 2024/03/29 AB An inherited red blood disorder characterized by chronic hemolytic anemia and intermittent vaso-occlusion resulting in tissue ischemia with acute severe pain, infections, congestive heart failure, cerebral infarction, kidney damage with bloody urine, splenomegaly, hepatomegaly and jaundice, eye damage, and bone marrow defects. The most common type is known as sickle cell anemia (SCA).