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Statements

Subject Item
n2:RIV%2F00159816%3A_____%2F10%3A%230000498%21RIV11-MZ0-00159816
rdf:type
n7:Vysledek skos:Concept
dcterms:description
Hereditary cancer syndromes are frequently seen in young cancer patients and patients with a positive family history. Genetic testing is important for the identifi cation of high-risk individuals, and for the early introduction of specialized preventive care or prophylactic surgeries. The use of genetic testing is increasing because of more frequent referrals from oncologists and other specialists and the increasing variety of genes tested. However, in some patients the testing is not recommended and other family members are dying because of the late diagnosis of hereditary syndrome. Greater awareness of the importance of genetic testing in oncology is needed. Hereditary cancer syndromes are frequently seen in young cancer patients and patients with a positive family history. Genetic testing is important for the identifi cation of high-risk individuals, and for the early introduction of specialized preventive care or prophylactic surgeries. The use of genetic testing is increasing because of more frequent referrals from oncologists and other specialists and the increasing variety of genes tested. However, in some patients the testing is not recommended and other family members are dying because of the late diagnosis of hereditary syndrome. Greater awareness of the importance of genetic testing in oncology is needed.
dcterms:title
Genetic testing and prevention of pereditary pancer at the MMCI - pver 10 years of experience Genetic testing and prevention of pereditary pancer at the MMCI - pver 10 years of experience
skos:prefLabel
Genetic testing and prevention of pereditary pancer at the MMCI - pver 10 years of experience Genetic testing and prevention of pereditary pancer at the MMCI - pver 10 years of experience
skos:notation
RIV/00159816:_____/10:#0000498!RIV11-MZ0-00159816
n4:aktivita
n15:P
n4:aktivity
P(NS10401)
n4:cisloPeriodika
6
n4:dodaniDat
n13:2011
n4:domaciTvurceVysledku
n16:9426272
n4:druhVysledku
n12:J
n4:duvernostUdaju
n11:S
n4:entitaPredkladatele
n10:predkladatel
n4:idSjednocenehoVysledku
260416
n4:idVysledku
RIV/00159816:_____/10:#0000498
n4:jazykVysledku
n17:eng
n4:klicovaSlova
hereditary cancer, syndromes, genes, genetic testing, prevention
n4:klicoveSlovo
n5:prevention n5:syndromes n5:genetic%20testing n5:genes n5:hereditary%20cancer
n4:kodStatuVydavatele
CZ - Česká republika
n4:kontrolniKodProRIV
[2FAB5F88E289]
n4:nazevZdroje
Klinická onkologie
n4:obor
n14:FD
n4:pocetDomacichTvurcuVysledku
1
n4:pocetTvurcuVysledku
10
n4:projekt
n9:NS10401
n4:rokUplatneniVysledku
n13:2010
n4:svazekPeriodika
23
n4:tvurceVysledku
Kalábová, R. Schneiderová, M. Svoboda, M. Krejčí, E. Petráková, K. Bolčák, K. Foretová, L. Palácová, M. Navrátilová, M. Dražan, Luboš
s:issn
0862-495X
s:numberOfPages
13