A case of sporadic Peutz-Jeghers syndrome presenting as multiple intussusceptions

Peutz-Jeghers syndrome (PJS) is an autosomal dominant mutation of the STK11/LKB1 gene on chromosome 19 often characterized by mucocutaneous pigmentation, hamartomatous polyps, anemia, gastrointestinal bleeding and intussusception. We present the case of a 21-year-old female with no pertinent family...

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Detalles Bibliográficos
Autores principales: Gorji, Leva, Huish, Grant, Morgan, Joshua, Levy, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8907407/
https://www.ncbi.nlm.nih.gov/pubmed/35280052
http://dx.doi.org/10.1093/jscr/rjac070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8907407/
https://www.ncbi.nlm.nih.gov/pubmed/35280052
http://dx.doi.org/10.1093/jscr/rjac070

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