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7/31/2024 3:54:54 AM | Browse: 280 | Download: 342
Publication Name World Journal of Clinical Cases
Manuscript ID 92220
Country China
Received
2024-01-19 07:24
Peer-Review Started
2024-01-19 07:24
To Make the First Decision
Return for Revision
2024-06-20 03:12
Revised
2024-06-24 07:27
Second Decision
2024-07-18 02:42
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2024-07-18 09:16
Articles in Press
2024-07-18 09:16
Publication Fee Transferred
2024-07-18 10:39
Edit the Manuscript by Language Editor
Typeset the Manuscript
2024-07-29 03:09
Publish the Manuscript Online
2024-07-31 02:48
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: http://creativecommons.org/Licenses/by-nc/4.0/
Copyright © The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Genetics & Heredity
Manuscript Type Case Report
Article Title HDR syndrome presented with nephrotic syndrome in a Chinese boy: A case report
Manuscript Source Unsolicited Manuscript
All Author List Li-Juan Ma, Wu Yang and Hong-Wen Zhang
Funding Agency and Grant Number
Corresponding Author Hong-Wen Zhang, MD, Chief Doctor, Department of Pediatric, Peking University First Hospital, No. 1 Xi’anmen Dajie, Beijing 100034, China. zhanghongwen@126.com
Key Words HDR syndrome; Sensorineural deafness; Nephrotic syndrome; China; Case report
Core Tip HDR syndrome is a rare genetic disease caused by variants in the GATA3 gene and is phenotypically defined by the triad of hypoparathyroidism (H), deafness (D), and renal disease (R). Patients with HDR syndrome may exhibit the full phenotypic triad or only a subset. Renal disorders of HDR are mainly developmental abnormalities, although renal functional abnormalities can also be observed. Nephrotic syndrome or nephrotic-level proteinuria is rare in HDR syndrome. Here, we report a Chinese infant with HDR syndrome who present with early-onset nephrotic syndrome.
Publish Date 2024-07-31 02:48
Citation <p>Ma LJ, Yang W, Zhang HW. HDR syndrome presented with nephrotic syndrome in a Chinese boy: A case report. <i>World J Clin Cases</i> 2024; 12(27): 6111-6116</p>
URL https://www.wjgnet.com/2307-8960/full/v12/i27/6111.htm
DOI https://dx.doi.org/10.12998/wjcc.v12.i27.6111
Full Article (PDF) WJCC-12-6111-with-cover.pdf
CARE Checklist–2016 92220-CARE-Checklist-2016.pdf
Manuscript File 92220_Auto_Edited_065958.docx
Answering Reviewers 92220-answering-reviewers.pdf
Audio Core Tip 92220-audio.mp3
Conflict-of-Interest Disclosure Form 92220-conflict-of-interest-statement.pdf
Copyright License Agreement 92220-copyright-assignment.pdf
Signed Consent for Treatment Form(s) or Document(s) 92220-informed-consent-statement.pdf
Non-Native Speakers of English Editing Certificate 92220-non-native-speakers.pdf
Peer-review Report 92220-peer-reviews.pdf
Scientific Misconduct Check 92220-scientific-misconduct-check.png
Scientific Editor Work List 92220-scientific-editor-work-list.pdf
CrossCheck Report 92220-crosscheck-report.pdf