• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

动脉肝发育不良:肝脏疾病与肺动脉狭窄以及面部和骨骼异常的关联。

Arteriohepatic dysplasia: association of liver disease with pulmonary arterial stenosis as well as facial and skeletal abnormalities.

作者信息

Levin S E, Zarvos P, Milner S, Schmaman A

出版信息

Pediatrics. 1980 Dec;66(6):876-83.

PMID:6450397
Abstract

The clinical features and course of five children with the recently described syndrome of arteriohepatic dysplasia are presented. All had bilateral pulmonary arterial stenosis, proven at cardiac catheterization, as well as associated liver disease of varying severity. In one of the fatal cases, a hitherto undescribed anomaly was found--stenosis of the right coronary artery ostium. A viral etiology, eg, the congenital rubella syndrome, was considered most likely, but detailed investigations proved to be negative.

摘要

本文介绍了最近描述的动脉肝发育不良综合征的5例患儿的临床特征及病程。所有患儿均经心导管检查证实有双侧肺动脉狭窄,以及不同程度的相关肝脏疾病。在其中1例死亡病例中,发现了一种此前未描述过的异常——右冠状动脉口狭窄。最有可能的病因是病毒感染,如先天性风疹综合征,但详细检查结果为阴性。

相似文献

1
Arteriohepatic dysplasia: association of liver disease with pulmonary arterial stenosis as well as facial and skeletal abnormalities.动脉肝发育不良:肝脏疾病与肺动脉狭窄以及面部和骨骼异常的关联。
Pediatrics. 1980 Dec;66(6):876-83.
2
Arteriohepatic dysplasia: phenotypic features and family studies.动脉肝发育不良:表型特征与家系研究。
Clin Genet. 1984 Apr;25(4):323-31. doi: 10.1111/j.1399-0004.1984.tb01998.x.
3
[Rubinstein-Taybi syndrome (a propos of 4 cases)].[鲁宾斯坦-泰比综合征(附4例报告)]
Arch Fr Pediatr. 1969 May;26(5):523-35.
4
Arteriohepatic dysplasia: familial pulmonary arterial stenosis with neonatal liver disease.动脉肝发育不良:伴有新生儿肝病的家族性肺动脉狭窄。
Arch Dis Child. 1973 Jun;48(6):459-66. doi: 10.1136/adc.48.6.459.
5
[Anomalous coronary drainage from the pulmonary artery with associated heart and vascular abnormalities. Report on 3 patients and review of the literature].[伴有相关心脏和血管异常的肺动脉异常冠状动脉引流。3例报告并文献复习]
Herz. 1983 Apr;8(2):93-104.
6
Arteriohepatic dysplasia (Alagille syndrome): extreme variability among affected family members.
Am J Med Genet. 1984 Oct;19(2):325-32. doi: 10.1002/ajmg.1320190215.
7
[Arteriohepatic dysplasia].[动脉肝发育不良]
Monatsschr Kinderheilkd (1902). 1976 May;124(5):382-3.
8
[Beuren-Williams syndrome: study of 20 cases].[贝伦-威廉姆斯综合征:20例研究]
An Esp Pediatr. 1986 May;24(5):291-7.
9
[Arteriohepatic dysplasia (author's transl)].肝动脉发育异常(作者译)
Leber Magen Darm. 1979 Sep;9(5):247-52.
10
A child with facial and skeletal dysmorphia reminiscent of Schwartz syndrome.
Birth Defects Orig Artic Ser. 1975;11(2):456-8.

引用本文的文献

1
Alagille syndrome.阿拉吉耶综合征
J Med Genet. 1997 Feb;34(2):152-7. doi: 10.1136/jmg.34.2.152.
2
Arteriohepatic dysplasia (Alagille's syndrome): unusual hepatic architecture and function.
Abdom Imaging. 1995 May-Jun;20(3):191-6. doi: 10.1007/BF00200391.
3
Investigation of serum bile acids; seven patients with Alagille syndrome.血清胆汁酸检测;7例阿拉吉耶综合征患者。
Eur J Pediatr. 1985 Sep;144(3):236-9. doi: 10.1007/BF00451949.
4
Glomerular mesangiolipidosis in Alagille syndrome (arteriohepatic dysplasia).阿拉吉耶综合征(动脉肝发育不良)中的肾小球系膜脂质沉积症。
Pediatr Nephrol. 1987 Jul;1(3):455-64. doi: 10.1007/BF00849254.
5
The Alagille syndrome (arteriohepatic dysplasia).阿拉吉耶综合征(动脉肝发育不良)。
J Med Genet. 1987 Oct;24(10):621-6. doi: 10.1136/jmg.24.10.621.