Results 1 to 10 of about 34,523 (140)

Use of family history taking for hereditary neoplastic syndromes screening in primary health care: A systematic review protocol.

open access: yesPLoS ONE, 2022
BackgroundAlthough most neoplasms result from complex interactions between the individual's genome and the environment, a percentage of cases is particularly due to inherited alterations that confer a greater predisposition to the development of tumors ...
Raphael Manhães Pessanha   +3 more
doaj   +3 more sources

Diagnostics of hereditary cancer syndromes by ngs. A database creation experience [PDF]

open access: yesКлиническая практика, 2021
Background: More than 500 thousand new cases of malignant neoplasms are registered annually in the Russian Federation, of which more than 50 thousand new cases are due to hereditary forms.
Ivan S. Abramov   +8 more
doaj   +1 more source

Lynch-like Syndrome and its Molecular Approaches: A Brief Report and Literature Review [PDF]

open access: yesMiddle East Journal of Cancer, 2023
Lynch syndrome (LS) predisposes individuals to early-onset colorectal and other Lynch-associated cancer. This disorder is an autosomal dominant genetic disturbance caused by germline mutations in one of the mismatch repair genes.
Zeinab Abdollahi   +3 more
doaj   +1 more source

Hereditary melanoma: a five-year study of Brazilian patients in a cancer referral center - phenotypic characteristics of probands and pathological features of primary tumors [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2018
: BACKGROUND: Approximately five to 10% of all melanomas occur in families with hereditary predisposition and the main high-risk melanoma susceptibility gene is the CDKN2A.
Bianca Costa Soares de Sá   +4 more
doaj   +2 more sources

Management of Patients with Hereditary Colorectal Cancer Syndromes

open access: yesGE: Portuguese Journal of Gastroenterology, 2015
Colorectal cancer (CRC) is one of the most important causes of death in the world. Hereditary CRC is found in 5–10% of CRC patients. In this review, we will focus on the major forms of hereditary CRC and their management according to the most recent ...
Catarina Brandão, Jorge Lage
doaj   +1 more source

Fibroblast growth factor receptor signaling in hereditary and neoplastic disease: biologic and clinical implications. [PDF]

open access: yes, 2015
Fibroblast growth factors (FGFs) and their receptors (FGFRs) are transmembrane growth factor receptors with wide tissue distribution. FGF/FGFR signaling is involved in neoplastic behavior and also development, differentiation, growth, and survival.
Helsten, Teresa   +2 more
core   +2 more sources

The role of hereditary colorectal cancer registries in identification of high risk patients and treatment improvement

open access: yesAlʹmanah Kliničeskoj Mediciny, 2018
Up to 10% of cases of sporadic colorectal cancer are considered to be related to hereditary genetic factors. The rates of colorectal cancer related to already identified genetic factors is about 5%.
D. Yu. Pikunov   +2 more
doaj   +1 more source

Cancer Predisposition Syndromes and Medulloblastoma in the Molecular Era

open access: yesFrontiers in Oncology, 2020
Medulloblastoma is the most common malignant brain tumor in children. In addition to sporadic cases, medulloblastoma may occur in association with cancer predisposition syndromes.
Roberto Carta   +18 more
doaj   +1 more source

Cutaneous Expression of Familial Cancer Syndromes

open access: yesActa Dermato-Venereologica, 2021
Genodermatoses are inherited syndromes with cutaneous manifestations. Some genodermatoses are associated with malignancy of internal organs and tissues.
Anne-Johanne Andersen   +3 more
doaj   +1 more source

Hereditary colorectal cancer: genetics and screening diagnostics

open access: yesРоссийский журнал гастроэнтерологии, гепатологии, колопроктологии, 2018
Aim of review. To present the data on main forms of hereditary colorectal cancer (CRC) and to discuss issues of its diagnostics, genetic testing and patient management. Summary.
O. I. Kit   +6 more
doaj   +1 more source

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