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7/31/2024 3:54:54 AM | Browse: 280 | Download: 342
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Received |
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2024-01-19 07:24 |
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2024-01-19 07:24 |
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2024-06-20 03:12 |
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Revised |
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2024-06-24 07:27 |
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Second Decision |
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2024-07-18 02:42 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2024-07-18 09:16 |
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Articles in Press |
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2024-07-18 09:16 |
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2024-07-18 10:39 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2024-07-29 03:09 |
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Publish the Manuscript Online |
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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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Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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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
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Manuscript Source |
Unsolicited Manuscript |
All Author List |
Li-Juan Ma, Wu Yang and Hong-Wen Zhang |
Funding Agency and Grant Number |
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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 |
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