一名患有呼吸急促、杵状指和中心性发绀的男孩。 - Suppr

Suppr

超能文献

A boy with breathlessness, digital clubbing and central cyanosis.

作者信息

Gordijn Sanne J, Brand Paul L P

机构信息

Department of Paediatrics, Isala Klinieken, 10500, 8000 GM Zwolle, The Netherlands.

出版信息

Eur J Pediatr. 2004 Feb;163(2):129-30. doi: 10.1007/s00431-003-1368-7. Epub 2003 Dec 3.

DOI:10.1007/s00431-003-1368-7

PMID:14652749

Abstract

摘要

相似文献

A boy with breathlessness, digital clubbing and central cyanosis.

Eur J Pediatr. 2004 Feb;163(2):129-30. doi: 10.1007/s00431-003-1368-7. Epub 2003 Dec 3.

Lupoid hepatitis, Rendu-Osler-Weber syndrome, clubbing cyanosis and hypertrophic osteoarthropathy.

J Med. 1975;6(3-4):291-301.

A rare case of congenital complex pulmonary AV fistula.

BMJ Case Rep. 2014 Oct 17;2014:bcr2014205939. doi: 10.1136/bcr-2014-205939.

Syndrome of cyanosis, digital clubbing, and hepatic disease in siblings.

J Pediatr. 1968 Jan;72(1):70-80. doi: 10.1016/s0022-3476(68)80402-0.

[A rare and little known cause of cyanosis: pulmonary arteriovenous aneurysm].

Ann Pediatr (Paris). 1991 Oct;38(8):572-5.

Pulmonary Arteriovenous Malformations in Dyskeratosis Congenita.

Pediatr Dermatol. 2015 Jul-Aug;32(4):e165-6. doi: 10.1111/pde.12589. Epub 2015 Apr 9.

Multiple intrapulmonary arteriovenous fistulas in childhood.

Pediatr Cardiol. 2000 Sep-Oct;21(5):493-6. doi: 10.1007/s002460010120.

Pulmonary arteriovenous fistula. A case-report with review of literature.

Indian Heart J. 1969 Apr;21(2):217-26.

An unusual cause of central cyanosis in a nine-year-old boy.

J Postgrad Med. 2012 Oct-Dec;58(4):314-7. doi: 10.4103/0022-3859.105468.

Cyanosis revealing hepatopulmonary syndrome in a child with dyskeratosis congenita.

Pediatr Pulmonol. 2010 Jan;45(1):99-102. doi: 10.1002/ppul.21128.

引用本文的文献

An update on the biology and management of dyskeratosis congenita and related telomere biology disorders.

Expert Rev Hematol. 2019 Dec;12(12):1037-1052. doi: 10.1080/17474086.2019.1662720. Epub 2019 Sep 10.

Pulmonary arteriovenous malformations: an uncharacterised phenotype of dyskeratosis congenita and related telomere biology disorders.

Eur Respir J. 2017 Jan 25;49(1). doi: 10.1183/13993003.01640-2016. Print 2017 Jan.

Hepatopulmonary syndrome is a frequent cause of dyspnea in the short telomere disorders.

Chest. 2015 Oct;148(4):1019-1026. doi: 10.1378/chest.15-0825.

本文引用的文献

Dyskeratosis congenita in all its forms.

Br J Haematol. 2000 Sep;110(4):768-79. doi: 10.1046/j.1365-2141.2000.02109.x.

Multiple intrapulmonary arteriovenous fistulas in childhood.

Pediatr Cardiol. 2000 Sep-Oct;21(5):493-6. doi: 10.1007/s002460010120.

Dyskeratosis Congenita (DC) Registry: identification of new features of DC.

Br J Haematol. 1998 Dec;103(4):990-6. doi: 10.1046/j.1365-2141.1998.01103.x.

Dyskeratosis congenita.

Dermatol Clin. 1995 Jan;13(1):33-9.

Dyskeratosis congenita.

J Med Genet. 1988 Dec;25(12):843-6. doi: 10.1136/jmg.25.12.843.

Bronchoalveolar disease in dyskeratosis congenita.

Eur Respir J. 1992 Apr;5(4):497-9.

Interstitial pulmonary disease associated with dyskeratosis congenita.

Am J Pediatr Hematol Oncol. 1992 Spring;14(1):89-92.

Dyskeratosis congenita: clinical and genetic heterogeneity. Report of a new case and review of the literature.

Am J Pediatr Hematol Oncol. 1992 Nov;14(4):297-304.

Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature.

J Med Genet. 1975 Dec;12(4):339-54. doi: 10.1136/jmg.12.4.339.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验