Hamilton W, Rosenthal A, Berwick D, Nadas A S
Pediatrics. 1978 Jun;61(6):911-4.
A 7-year-old black boy with sickle cell disease, Wolff-Parkinson-White syndrome, mild left ventricular dysfunction, and normal coronary arteries developed angina pectoris five months after cessation of hypertransfusion therapy. Exercise-induced ECG ST segment depression associated with angina disappeared following transfusion therapy.
一名患有镰状细胞病、 Wolff-Parkinson-White综合征、轻度左心室功能不全且冠状动脉正常的7岁黑人男孩，在停止高输血疗法五个月后出现了心绞痛。输血治疗后，与心绞痛相关的运动诱发的心电图ST段压低消失。
