Alagille syndrome

Harshalee Shendge; Milind S. Tullu; Asha Shenoy; Rachana Chaturvedi; Jaishree R. Kamat; Manisha Khare; Amita Joshi

首页> 外文期刊>The Indian Journal of Pediatrics >Alagille syndrome

【24h】

Alagille syndrome

机译：阿拉吉勒综合征

获取原文

获取原文并翻译 | 示例

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

摘要
著录项
相似文献
相关主题

摘要

Syndromic paucity of bile ducts or “Alagille syndrome” is characterized by peculiar facies, chronic cholestasis, posterior embryotoxon, butterfly-like vertebral arch defects and peripheral pulmonary artery hypopiasia or stenosis. We present a two-year-old female child with the ‘partial’ or ‘incomplete’ Alagille syndrome. The child had three of the five major features of the syndrome. A brief review of literature of the syndrome is presented.

机译：胆管综合征或“ Alagille综合征”的症状少见的特征是奇特的相，慢性胆汁淤积症，后胚胎毒素，蝴蝶样椎弓弓缺损和周围肺动脉发育不全或狭窄。我们介绍了一个两岁的女孩，患有“部分”或“不完整”的Alagille综合征。这个孩子患有该综合征的五个主要特征中的三个。简要介绍了该综合征的文献。

著录项

来源
《The Indian Journal of Pediatrics》 |2002年第9期|825-827|共3页
作者
Harshalee Shendge; Milind S. Tullu; Asha Shenoy; Rachana Chaturvedi; Jaishree R. Kamat; Manisha Khare; Amita Joshi;
展开▼
作者单位

Departments of Pediatrics Seth G. S. Medical College and KEM Hospital;

Departments of Pediatrics Seth G. S. Medical College and KEM Hospital;

Departments of Pathology Seth G. S. Medical College and KEM Hospital;

Departments of Pathology Seth G. S. Medical College and KEM Hospital;

Departments of Pediatrics Seth G. S. Medical College and KEM Hospital;

Departments of Pathology Seth G. S. Medical College and KEM Hospital;

Departments of Pathology Seth G. S. Medical College and KEM Hospital;

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类
关键词
Artehohepatic dysplasia; Bilirubin; Cholestasis; Embryotoxon; Pulmonary stenosis; Vertebral defects;

机译：大肠肝异型增生;胆红素;胆汁淤积;胚胎毒素;肺狭窄;椎骨缺损;

相似文献

外文文献
中文文献
专利

1. Outcomes of liver transplantation for Alagille syndrome after Kasai portoenterostomy: Alagille Syndrome with agenesis of extrahepatic bile ducts at porta hepatis [J] . Gunadi, Kaneshiro Masakatshu, Okamoto Tatsuya, Journal of Pediatric Surgery: Official Journal of the Surgical Section of the American Academy of Pediatric, the British Association of Paediatric Surgeons, the American Pediatric Surgical Association, and the Canadian Association of Paediatric Surgeons . 2019,第11期

机译：Kasai Portoenterostomy术后Alagille综合征的肝移植结果：Alagille综合征，Porta Hepatis患者癫痫患者癫痫病毒
2. Williams syndrome presenting with findings consistent with Alagille syndrome [J] . Binita Kamath, Hilary Whyte, Nicole Martin, Clinical Case Reports . 2015,第1期

机译：威廉姆斯综合征表现出与阿拉吉勒综合征一致的发现
3. Moyamoya Syndrome Associated with Alagille Syndrome: Outcome after Surgical Revascularization [J] . Baird Lissa C., Smith Edward R., Ichord Rebecca, The Journal of pediatrics . 2015,第2期

机译：Moyamoya综合征与Alagille综合征相关：手术血运重建后的结果。
4. A Fuzzy Model of Diagnosis of Eight Syndromes and Internal Organs' Syndromes in Traditional Vietnamese Medicine [C] . Nguyen Hoang Phuong International Conference on Frontiers of Intelligent Computing : Theory and Applications . 2020

机译：传统越南医学诊断八综合征诊断模糊模型及内部器官综合征
5. Pediatric Germline Predispositions to Myelodisplastic Syndrome, Expert Guidance for the Initial Evaluation and Management of SAMD9 and SAMD9L Variants, and the Importance of Database Development for These Rare Syndromes [D] . Nelson, Catherine. 2021

机译：小儿种芽髓倾向于骨髓性综合征，初步评估和管理的专家指导和SAMD9和SAMD9L变体的重要性，以及数据库开发对这些罕见综合征的重要性
6. Molecular analysis of 24 Alagille syndrome families identifies a single submicroscopic deletion and further localizes the Alagille region within 20p12. [O] . E B Rand, N B Spinner, D A Piccoli, 1995

机译：对24个Alagille综合征家族的分子分析确定了单个亚显微缺失并将Alagille区域进一步定位在20p12内。
7. Alagille syndrome and non-syndromic paucity of the intrahepatic bile ducts [O] . Melissa A. Gilbert, Kathleen M. Loomes 2021

机译：Alagille综合征和肝内胆管的非综合征缺乏

Alagille syndrome

摘要

著录项

相似文献

相关主题

期刊订阅