BPG is committed to discovery and dissemination of knowledge
Articles Published Processes
5/30/2025 10:57:27 AM | Browse: 195 | Download: 500
 |
Received |
|
2025-03-19 13:04 |
|
Peer-Review Started |
|
2025-03-19 13:04 |
|
First Decision by Editorial Office Director |
|
2025-03-28 01:34 |
|
Return for Revision |
|
2025-03-30 01:07 |
|
Revised |
|
2025-04-12 04:42 |
|
Publication Fee Transferred |
|
2025-04-14 08:25 |
|
Second Decision by Editor |
|
2025-05-09 02:46 |
 |
Second Decision by Editor-in-Chief |
|
|
|
Final Decision by Editorial Office Director |
|
2025-05-09 08:29 |
|
Articles in Press |
|
2025-05-09 08:29 |
|
Edit the Manuscript by Language Editor |
|
|
|
Typeset the Manuscript |
|
2025-05-26 01:30 |
|
Publish the Manuscript Online |
|
2025-05-30 10:57 |
| ISSN |
1948-9366 (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 |
Genetics & Heredity |
| Manuscript Type |
Case Report |
| Article Title |
Hereditary chronic intestinal pseudo-obstruction caused by a rare MYH11 mutation: A case report
|
| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Shan Jiang, Ya-Xuan Zhou, Xiao-Hong Sun, Pei-Pei Chen, Hao Tang, Yang Chen, Ya-Ping Liu, Yi-Xuan Li and Lin Kang |
| ORCID |
|
| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| National High Level Hospital Clinical Research Funding |
2022-PUMCH-B-129 |
|
| Corresponding Author |
Lin Kang, Chief Physician, MD, PhD, Department of Geriatrics, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, No 1 Shuaifuyuan, Dongcheng District, Beijing 100730, China. kangl@pumch.cn |
| Key Words |
Rare disease; Chronic intestinal pseudo-obstruction; Gastrointestinal motility disorder; MYH11; Case report |
| Core Tip |
Chronic intestinal pseudo-obstruction (CIPO) is a rare disorder, characterized by severe impairments of gastrointestinal motility. This case involves an elderly male with an insidious onset during adolescence and a disease course spanning several decades, who experienced two episodes of intestinal obstruction requiring ileocecal resection. The histopathological findings confirmed the diagnosis of CIPO. Whole-exome sequencing identified a rare heterozygous MYH11 mutation [NM_001040113.2: C.5819del (p.Pro1940HisfsTer91)], confirming the diagnosis of hereditary myopathic CIPO. This case provides evidence to support the role of MYH11 variants in the CIPO phenotype. |
| Publish Date |
2025-05-30 10:57 |
| Citation |
Jiang S, Zhou YX, Sun XH, Chen PP, Tang H, Chen Y, Liu YP, Li YX, Kang L. Hereditary chronic intestinal pseudo-obstruction caused by a rare MYH11 mutation: A case report. World J Gastrointest Surg 2025; 17(6): 107235 |
| URL |
https://www.wjgnet.com/1948-9366/full/v17/i6/107235.htm |
| DOI |
https://dx.doi.org/10.4240/wjgs.v17.i6.107235 |
All content on this site: Copyright © 1993-2026 Baishideng Publishing Group Inc, its licensors, and contributors. All rights are reserved, including those for text and data mining, AI training, and similar technologies. For all open access content, the relevant licensing terms apply.
