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Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control.

Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control. Research Abstract Details 

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  • Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control. Abstract Text:

    henry t lynchHenry T Lynch,ramon m fusaroRamon M Fusaro,jane f lynchJane F Lynch,

    Oncologists who are aware of the progress in hereditary cancer syndrome diagnosis, and, in particular, of how this effort may be effectively facilitated through a comprehensive family history in concert with molecular genetic studies, are in the envious position of designing highly targeted screening and management programs for the membership of these cancer-prone families. The Lynch syndrome is discussed as a clinical model wherein the presence of mismatch repair mutations provides a high level of diagnostic certainty for the initiation of targeted cancer screening and management. The familial atypical multiple mole melanoma-pancreatic cancer (FAMMM-PC) syndrome, on the other hand, provides another model with cancer-control potential. Given its phenotypic features of multiple atypical nevi, high total body mole count and cutaneous malignant melanoma, coupled with the integral association of PC in a subset of FAMMM kindreds with the CDKN2A germline mutation, this may result in a perhaps lower level of diagnostic certainty when compared with the Lynch syndrome. This knowledge may impact upon progress in the earlier diagnosis of melanoma and provide an impetus for creative diagnostic methods in PC, a disease that, at this time, demonstrates a mortality rate virtually identical to its incidence rate.

    Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control. Publishing Authors By Initials

    ht lynchHT Lynch,rm fusaroRM Fusaro,jf lynchJF Lynch,

    For similar neoplasms: neoplasms by site: digestive system neoplasms: pancreatic neoplasms research abstracts see: neoplasms: neoplasms by site: digestive system neoplasms: pancreatic neoplasms research

    PUBMED ID PMID:

    MEDLINE DATE:

    Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control. Journal Published:

    PUBLICATION TYPE: Review

    Journal: Future oncology (London, England)

    VOLUME: 3

    Page Numbers: 169-81

    Journal Abbreviation:

    ISSN: 1479-6694

    DAY: 3

    MONTH: Apr

    YEAR: 2007

    Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control. Information

    Number of References: 69

    LANGUAGE: eng

    NlmUniqueID: 101256629

    Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control. Keywords Mesh Terms:

    KEYWORDS: Pancreatic Neoplasms

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control. Information

    Substance Name: Cyclin-Dependent Kinase Inhibitor p16

    Registry Number: 0

    Grant and Affiliation Information for Hereditary cancer syndrome diagnosis: molecular genetic clues and cancer control.

    AFFILIATION: Department of Preventive Medicine, Creighton University School of Medicine, Omaha NE 68178, USA. htlynch@creighton.edu

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY: United States NCI

    GRANT: 1U01 CA 86389

    ACRONYM: CA

    MEDLINETA: Future Oncol

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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