Clinical studyScreening for hereditary non-polyposis colorectal cancer: A study of 22 kindreds in The Netherlands
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Molecular basis of diseases of the gastrointestinal tract
2018, Molecular Pathology: The Molecular Basis of Human DiseaseSurgical management for advanced duodenal adenomatosis and duodenal cancer in Dutch patients with familial adenomatous polyposis: A nationwide retrospective cohort study
2012, SurgeryCitation Excerpt :In 1985, the Netherlands Foundation for Detection of Hereditary Tumours (NFDHT) started a registry of patients with FAP. The main objectives of this nationwide polyposis registry are coordination of lifelong surveillance of at-risk patients and promotion of early detection of cancer in high-risk families.29 Patients with FAP are referred to this national registry by gastroenterologists, surgeons, or clinical geneticists.
Risk and Epidemiological Time Trends of Gastric Cancer in Lynch Syndrome Carriers in The Netherlands
2010, GastroenterologyCitation Excerpt :In the Netherlands, families with Lynch syndrome are registered at the nationwide Dutch Hereditary Cancer registry. A detailed description of the registry's approach has been described elsewhere.12 Briefly, families suspected for Lynch syndrome are referred by specialists and genetic centers to the registry from all parts of the Netherlands.
Sebaceous lesions and their associated syndromes: Part II
2009, Journal of the American Academy of DermatologyCitation Excerpt :Key points For patients with Lynch syndrome, intensive cancer screening has been shown to lead to the detection of colorectal cancers at an earlier stage than historical controls.123,148-156 It is likely that patients with MTS would also benefit from the same intensive screening as Lynch syndrome patients.