Presymptomatic genetic diagnosis of two siblings with hereditary angioedema, presenting with unusual normal levels of serum C4-Reference-Cited by-同舟云学术

Presymptomatic genetic diagnosis of two siblings with hereditary angioedema, presenting with unusual normal levels of serum C4

Published:2017-10-23 Issue:2 Volume:45 Page:e31-32
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Kasami Sachie¹,Sowa-Osako Junko¹^ORCID,Fukai Kazuyoshi¹^ORCID,Tokimasa Sadao²,Kaga Shin-ichiro³,Saito Ryo⁴,Tanaka Akio⁵,Hide Michihiro⁵,Tsuruta Daisuke¹

Affiliation:

1. Department ofDermatology; Osaka City University Graduate School of Medicine; Osaka Japan

2. Department of Pediatrics; Osaka City University Graduate School of Medicine; Osaka Japan

3. Department ofTrauma and Critical Care Medicine; Osaka City University Graduate School of Medicine; Osaka Japan

4. Department of Dermatology; University Hospital; Hiroshima University; Hiroshima Japan

5. Department of Dermatology; Institute of Biomedical and Health Sciences Hiroshima University; Hiroshima Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.14103/fullpdf

Reference5 articles.

1. Hereditary angioedema as the cause of death from asphyxia: postmortem computed tomography study;Shibuya;Allergol Int,2014

2. Mutational spectrum and phenotypes in Danish families with hereditary angioedema because of C1 inhibitor deficiency;Bygum;Allergy,2011

3. Novel and recurrent C1 inhibitor gene mutations in nine Japanese patients with hereditary angioedema;Iwamoto;J Dermatol Sci,2012

4. Mutation screening of the C1 inhibitor gene among Hungarian patients with hereditary angioedema;Kalmár;Hum Mutat,2003

5. Clinical and laboratory characteristics that differentiate hereditary angioedema in 72 patients with angioedema;Ohsawa;Allergol Int,2014

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. International Consensus on the Use of Genetics in the Management of Hereditary Angioedema;The Journal of Allergy and Clinical Immunology: In Practice;2020-03

2. Targeted next-generation sequencing for the molecular diagnosis of hereditary angioedema due to C1-inhibitor deficiency;Gene;2018-08