Pregled bibliografske jedinice broj: 430394
Cytogenetics and molekular findings in childhood leukemia of South Croatia
Cytogenetics and molekular findings in childhood leukemia of South Croatia // Hrvatski kongres kliničke citologije 1. Hrvatski simpozij analitičke citologije 2. Hrvatski simpozij citotehnologije, Split. October 11-14, 2009. Konačni program i knjiga sažetaka
Zagreb, 2009. str. 165-165 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 430394 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Cytogenetics and molekular findings in childhood leukemia of South Croatia
Autori
Lozić Bernarda, Čulić Srđana, Čulić Vida, Drmić Irena, Batinić Drago, Mrsić Sanja, Lasan Trčić Ružica, Zemunik Tatjana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Hrvatski kongres kliničke citologije 1. Hrvatski simpozij analitičke citologije 2. Hrvatski simpozij citotehnologije, Split. October 11-14, 2009. Konačni program i knjiga sažetaka
/ - Zagreb, 2009, 165-165
Skup
4. Hrvatski kongres kliničke citologije 1. Hrvatski simpozij analitičke citologije 2. Hrvatski simpozij citotehnologije, Split. October 11-14, 2009
Mjesto i datum
Split, Hrvatska, 11.10.2009. - 14.10.2009
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
cytogenetics; molecular genetics; childhood; leukemia
Sažetak
The aim of this study was to identify cytogenetic and molecular findings among the major pediatric leukemia in South Croatia. Leukemia is most common malignant disease in childhood and presents approximately 25% of all childhood cancer. This study showed the incidence of 3, 2 new cases of acute leukemia per 100000 children under the age of 18 years in our population. Immunophenotype characteristics of the 27(82%) pediatric patients with ALL and 6 patients with AML (18%) were analyzed. The most frequent abnormalities found in ALL were different abnormalities of chromosome short arm 9p (3/24 cases) and between AML it was t(8 ; 21)(q22 ; q22) (2/6). The most frequent gene rearangement was TEL/AML1 in 14/27 (51.5%) of all ALL cases. Due to the small number of patients in each genetic subgroup and short time of their follow-up, we could not analyze the relationship between the outcome and each gene rearrangement.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-0000000-0049 - Zloćudne bolesti u djece (Konja, Josip, MZOS ) ( CroRIS)
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta,
Medicinski fakultet, Zagreb,
Medicinski fakultet, Split