Must Peutz-Jeghers syndrome patients have the LKB1/STK11 gene mutation? A case report and review of the literature

doi:10.12998/wjcc.v6.i8.224

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Aug 16, 2018 (publication date) through May 17, 2024

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World Journal of Clinical Cases

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2307-8960

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

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World J Clin Cases. Aug 16, 2018; 6(8): 224-232
Published online Aug 16, 2018. doi: 10.12998/wjcc.v6.i8.224

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Figure 1 Mucocutaneous pigmentation of the patient.

Citation: Duan FX, Gu GL, Yang HR, Yu PF, Zhang Z. Must Peutz-Jeghers syndrome patients have the LKB1/STK11 gene mutation? A case report and review of the literature. World J Clin Cases 2018; 6(8): 224-232
URL: https://www.wjgnet.com/2307-8960/full/v6/i8/224.htm
DOI: https://dx.doi.org/10.12998/wjcc.v6.i8.224