BPG is committed to discovery and dissemination of knowledge
Articles Published Processes
4/27/2025 7:06:36 AM | Browse: 2 | Download: 0
Publication Name World Journal of Clinical Cases
Manuscript ID 104723
Country Türkiye
Received
2024-12-31 03:04
Peer-Review Started
2024-12-31 03:05
To Make the First Decision
Return for Revision
2025-03-12 06:50
Revised
2025-03-12 12:34
Second Decision
2025-03-19 02:39
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2025-03-21 02:15
Articles in Press
2025-03-21 02:15
Publication Fee Transferred
Edit the Manuscript by Language Editor
2025-03-25 00:02
Typeset the Manuscript
2025-04-16 10:27
Publish the Manuscript Online
2025-04-27 07:06
ISSN 2307-8960 (online)
Open Access This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Copyright © The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Allergy
Manuscript Type Minireviews
Article Title Hereditary alpha tryptasemia and clinical implications
Manuscript Source Invited Manuscript
All Author List Ece Tüsüz Önata, Öner Özdemir and Süreyya Savaşan
ORCID
Author(s) ORCID Number
Öner Özdemir http://orcid.org/0000-0002-5338-9561
Funding Agency and Grant Number
Corresponding Author Öner Özdemir, MD, Professor, Division of Allergy and Immunology, Department of Pediatrics, Sakarya Research and Training Hospital, Sakarya University, Faculty of Medicine, Adnan Menderes Cad, Sağlık Sok, 195 Adapazarı, Sakarya 54100, Türkiye. onerozdemir@sakarya.edu.tr
Key Words Tryptasemia; Autosomal dominant; Hereditary alpha tryptasemia; Mast cell; Tyrosine kinase protein
Core Tip Hereditary alpha tryptasemia was described in 2016 and is the most common (up to 72%) cause of elevated serum basal tryptase (TPS). The clinical presentation of this condition, which is caused by copy number gains in the TPSAB1 gene encoding serum α TPS, is variable for each patient.
Publish Date 2025-04-27 07:06
Citation <p>Tüsüz Önata E, Özdemir Ö, Savaşan S. Hereditary alpha tryptasemia and clinical implications. <i>World J Clin Cases</i> 2025; 13(21): 104723</p>
URL https://www.wjgnet.com/2307-8960/full/v13/i21/104723.htm
DOI https://dx.doi.org/10.12998/wjcc.v13.i21.104723
Full Article (PDF) WJCC-13-104723-with-cover.pdf
Manuscript File 104723_Auto_Edited_062915.docx
Answering Reviewers 104723-answering-reviewers.pdf
Audio Core Tip 104723-audio.mp4
Conflict-of-Interest Disclosure Form 104723-conflict-of-interest-statement.pdf
Copyright License Agreement 104723-copyright-assignment.pdf
Non-Native Speakers of English Editing Certificate 104723-non-native-speakers.pdf
Peer-review Report 104723-peer-reviews.pdf
Scientific Misconduct Check 104723-scientific-misconduct-check.png
Scientific Editor Work List 104723-scientific-editor-work-list.pdf
CrossCheck Report 104723-crosscheck-report.pdf