Intensive surveillance endoscopy for multiple gastrointestinal tumors in a patient with constitutional mismatch repair deficiency: case report

BACKGROUND: Constitutional mismatch repair deficiency (CMMRD) is an extremely rare autosomal recessive hereditary disease characterized by the absence of mismatch repair gene activity from birth, which results in brain tumors, colonic polyposis, gastrointestinal cancers, and lymphomas later in life....

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Detalles Bibliográficos
Autores principales: Ando, Takayuki, Nakajima, Takahiko, Fukuda, Rei, Nomura, Keiko, Niida, Yo, Sakumura, Miho, Motoo, Iori, Mihara, Hiroshi, Nanjo, Sohachi, Kajiura, Shinya, Fujinami, Haruka, Hojo, Shojo, Fujii, Tsutomu, Yasuda, Ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381554/
https://www.ncbi.nlm.nih.gov/pubmed/34425783
http://dx.doi.org/10.1186/s12876-021-01902-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381554/
https://www.ncbi.nlm.nih.gov/pubmed/34425783
http://dx.doi.org/10.1186/s12876-021-01902-6

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