Advance in research on the correlation between genotypes of susceptible mutations and clinical phenotype of familial adenomatous polyposis / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
;
(6): 919-923, 2017.
Artículo
en Chino
| WPRIM
| ID: wpr-344145
ABSTRACT
Familial adenomatous polyposis (FAP) is one of the most common hereditary colorectal cancers. Its intestinal and extra-intestinal manifestations are correlated with mutation sties of the APC gene. Potential gene modulation sites in patients who have typical clinical manifestations but with unidentified APC mutations are also discussed, which included MUTYH gene, AXIN gene and certain epigenetic changes. With the generalization of Precision Medicine, to offer individualized treatment and surveillance strategy based on the genotype-phenotype correlation will be of great value for FAP patients. This review focuses on the research advance in genotype - phenotype correlation studies of FAP patients.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Genes APC
/
Poliposis Adenomatosa del Colon
/
Predisposición Genética a la Enfermedad
/
ADN Glicosilasas
/
Beta Catenina
/
Estudios de Asociación Genética
/
Proteína Axina
/
Genética
/
Mutación
Límite:
Humanos
Idioma:
Chino
Revista:
Chinese Journal of Medical Genetics
Año:
2017
Tipo del documento:
Artículo
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