Hereditary chronic intestinal pseudo-obstruction caused by a rare MYH11 mutation: A case report

doi:10.4240/wjgs.v17.i6.107235

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Jun 27, 2025 (publication date) through Jun 5, 2025

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World Journal of Gastrointestinal Surgery

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1948-9366

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastrointest Surg. Jun 27, 2025; 17(6): 107235
Published online Jun 27, 2025. doi: 10.4240/wjgs.v17.i6.107235

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Figure 5 Sanger sequencing validation of the mutation site in myosin (MYH11; NM_001040113. 2: C.5819del (p.Pro1940HisfsTer91). The top and bottom plots show the verification for the patient and the patient’s son, respectively. The red arrow indicates the mutation location, at the C nucleotide at position 5819 of the gene coding sequence.

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