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Origin of the left coronary artery from the right pulmonary artery and ventricular septal defect in a child of a mother with raised plasma phenylalanine concentrations throughout pregnancy.一名母亲在整个孕期血浆苯丙氨酸浓度升高,其孩子出现左冠状动脉起源于右肺动脉及室间隔缺损。
Br Heart J. 1990 Mar;63(3):180-2. doi: 10.1136/hrt.63.3.180.
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Anomalous origin of single coronary artery from pulmonary artery: serendipitous diagnosis and successful surgical treatment.单一冠状动脉起源于肺动脉的异常情况:偶然诊断与成功手术治疗
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Anomalous origin of the left coronary artery from the right pulmonary artery associated with ventricular septal defect.左冠状动脉起源于右肺动脉并伴有室间隔缺损
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引用本文的文献

1
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature.母体苯丙酮尿症与子代结局:一项回顾性研究及文献系统综述
Nutrients. 2025 Feb 14;17(4):678. doi: 10.3390/nu17040678.
2
Cardiac defects in the children of mothers with high concentrations of plasma phenylalanine.血浆苯丙氨酸浓度高的母亲所生子女的心脏缺陷
Br Heart J. 1990 Mar;63(3):143-4. doi: 10.1136/hrt.63.3.143.

本文引用的文献

1
Maternal phenylketonuria and hyperphenylalaninemia. An international survey of the outcome of untreated and treated pregnancies.母体苯丙酮尿症和高苯丙氨酸血症。未经治疗和经治疗妊娠结局的国际调查。
N Engl J Med. 1980 Nov 20;303(21):1202-8. doi: 10.1056/NEJM198011203032104.
2
Maternal hyperphenylalaninemia fetal effects.母体高苯丙氨酸血症对胎儿的影响。
J Pediatr. 1984 Feb;104(2):216-20. doi: 10.1016/s0022-3476(84)80995-6.
3
Anomalous origin of the left coronary artery from the right pulmonary artery associated with ventricular septal defect.左冠状动脉起源于右肺动脉并伴有室间隔缺损
Chest. 1970 Dec;58(6):616-20. doi: 10.1378/chest.58.6.616.
4
Origin of the left coronary artery from the right pulmonary artery: a report of successful surgery in a 3-month-old child.左冠状动脉起源于右肺动脉:一名3个月大儿童成功手术的报告。
Ann Thorac Surg. 1986 Apr;41(4):446-8. doi: 10.1016/s0003-4975(10)62708-7.
5
[Embryofetopathy caused by postnatally detected maternal phenylketonuria].[产后检测出的母体苯丙酮尿症所致胚胎病]
Helv Paediatr Acta. 1987 Jun;42(5-6):463-9.
6
Origin of anterior descending branch of left coronary artery from pulmonary trunk.左冠状动脉前降支起源于肺动脉干。
Br Heart J. 1976 May;38(5):523-5. doi: 10.1136/hrt.38.5.523.
7
Anomalous origin of the left coronary artery from the right pulmonary artery.左冠状动脉起源于右肺动脉异常。
J Thorac Cardiovasc Surg. 1976 May;71(5):787-91.
8
Anomalous origin of left coronary artery from the pulmonary artery with ventricular septal defect.左冠状动脉起源于肺动脉伴室间隔缺损
Circulation. 1978 May;57(5):1026-30. doi: 10.1161/01.cir.57.5.1026.
9
Anomalous origin of left coronary artery from pulmonary artery in association with intracardiac lesions. Report of two cases.左冠状动脉起源于肺动脉并合并心内病变。两例报告。
J Thorac Cardiovasc Surg. 1979 Jul;78(1):12-20.
10
Anomalous left coronary artery originating from the pulmonary artery. Report on 15 cases.
Circulation. 1975 Jun;51(6):976-87. doi: 10.1161/01.cir.51.6.976.

一名母亲在整个孕期血浆苯丙氨酸浓度升高,其孩子出现左冠状动脉起源于右肺动脉及室间隔缺损。

Origin of the left coronary artery from the right pulmonary artery and ventricular septal defect in a child of a mother with raised plasma phenylalanine concentrations throughout pregnancy.

作者信息

Henglein D, Niederhoff H, Bode H

机构信息

Department of Paediatric Cardiology, University of Freiburg, Federal Republic of Germany.

出版信息

Br Heart J. 1990 Mar;63(3):180-2. doi: 10.1136/hrt.63.3.180.

DOI:10.1136/hrt.63.3.180
PMID:2328170
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1024400/
Abstract

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.

摘要

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。