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

Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disease, which is characterized by mucocutaneous pigmentation and multiple gastrointestinal hamartoma polyps. The germline mutation of LKB1/STK11 gene on chromosome 19p13.3 is considered to be the hereditary cause of PJS. However, must...

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Detalles Bibliográficos
Autores principales: Duan, Fu-Xiao, Gu, Guo-Li, Yang, Hai-Rui, Yu, Peng-Fei, Zhang, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107527/
https://www.ncbi.nlm.nih.gov/pubmed/30148152
http://dx.doi.org/10.12998/wjcc.v6.i8.224

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107527/
https://www.ncbi.nlm.nih.gov/pubmed/30148152
http://dx.doi.org/10.12998/wjcc.v6.i8.224

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