Henglein D, Niederhoff H, Bode H
Department of Paediatric Cardiology, University of Freiburg, Federal Republic of Germany.
Br Heart J. 1990 Mar;63(3):180-2. doi: 10.1136/hrt.63.3.180.
A child with anomalous origin of the left coronary artery from the right pulmonary artery, ventricular septal defect, fetal growth retardation, and facial abnormalities was born to a woman in whom plasma phenylalanine concentrations had been raised throughout pregnancy. The cardiac abnormalities were diagnosed by angiography when the child was eight months old. The anomalous coronary artery was imaged in a subsequent echocardiogram. Development retardation was caused by maternal phenylketonuria, which may also have been responsible for the development of the ventricular septal defect and the coronary anomaly. If dietary treatment of the mother had been started before pregnancy damage to the child might have been prevented.
一名左冠状动脉起源于右肺动脉、患有室间隔缺损、胎儿生长受限和面部畸形的儿童,其母亲在整个孕期血浆苯丙氨酸浓度均升高。该儿童八个月大时通过血管造影诊断出心脏异常。随后的超声心动图对异常冠状动脉进行了成像。发育迟缓是由母体苯丙酮尿症引起的,这也可能是室间隔缺损和冠状动脉异常发展的原因。如果在怀孕前就开始对母亲进行饮食治疗,可能会防止对孩子造成损害。