Síndrome de Lynch: genética y cirugía / Lynch syndrome: genetics and surgery
Cir. Esp. (Ed. impr.)
; 89(1): 3-9, ene. 2011. graf, tab, ilus
Article
in Spanish
| IBECS
| ID: ibc-95662
Responsible library:
ES1.1
Localization: BNCS
RESUMEN
El cáncer colorrectal hereditario no polipósico o síndrome de Lynch, causado por mutaciones germinales en genes reparadores de bases desapareadas de ácido desoxirribonucleico (ADN), es la forma más frecuente de cáncer colorrectal hereditario. La identificación de estos individuos no es fácil y se basa en criterios clínicos y moleculares. Se expone a continuación una revisión sobre genética y diagnóstico en el síndrome de Lynch, así como sobre su manejo quirúrgico y prevención (AU)
ABSTRACT
Hereditary nonpolyposis colorectal cancer or Lynch Syndrome, caused by germinal mutations in mismatch deoxyribonucleic acid (DNA) repair genes, is the most common form of hereditary colorectal cancer. The identification of these individuals is not easy and is based on clinical and molecular criteria. A review is presented on the genetics and diagnosis in Lynch Syndrome, as well as on its surgical management and prevention (AU)
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Collection:
National databases
/
Spain
Health context:
SDG3 - Health and Well-Being
Health problem:
Target 3.4: Reduce premature mortality due to noncommunicable diseases
Database:
IBECS
Main subject:
Colorectal Neoplasms, Hereditary Nonpolyposis
/
Mass Screening
Type of study:
Prognostic study
/
Screening study
Limits:
Humans
Language:
Spanish
Journal:
Cir. Esp. (Ed. impr.)
Year:
2011
Document type:
Article
Institution/Affiliation country:
Hospital Torrecárdenas/España