Hereditary chronic intestinal pseudo-obstruction caused by a rare <i>MYH11</i> mutation: A case report
This report adds to our current understanding of CIPO etiology by reinforcing the role of <i>MYH11</i> variants in the pathogenesis of the CIPO phenotype.
Authors
- Lin Kang (ORCID: https://orcid.org/0000-0002-9186-9574)
- Yi Zhou (ORCID: https://orcid.org/0000-0001-9024-7514)
- Yixuan Li (ORCID: https://orcid.org/0000-0002-8000-3417)
- Shan Jiang (ORCID: https://orcid.org/0000-0003-1265-4776)
- Chen Yang (ORCID: https://orcid.org/0000-0001-6011-4067)
- Yaping Liu (ORCID: https://orcid.org/0000-0003-2680-4536)
- Hao Tang
- Peipei Chen (ORCID: https://orcid.org/0000-0002-4823-7176)
- Xiaohong Sun
Institutions
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Peking Union Medical College Hospital (CN)
Publication Details
- Journal
- World Journal of Gastrointestinal Surgery
- Published
- 2025-05-29
- DOI
- https://doi.org/10.4240/wjgs.v17.i6.107235
- Primary Topic
- Congenital gastrointestinal and neural anomalies
- Type
- article
- Field-Weighted Citation Impact
- 0.00