Pregled bibliografske jedinice broj: 318175
Cytogenetic and chromosome Y microdeletion analysis of infertile men from North-Adriatic region of Croatia
Cytogenetic and chromosome Y microdeletion analysis of infertile men from North-Adriatic region of Croatia // European Journal of Human Genetics, vol 13 - suppl 1
Prag, Češka Republika, 2005. str. 107-107 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 318175 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Cytogenetic and chromosome Y microdeletion analysis of infertile men from North-Adriatic region of Croatia
Autori
Buretić-Tomljanović, Alena ; Vlastelić, Ivan ; Ostojić, Saša ; Vraneković, Jadranka ; Randić Ljiljana , Kapović, Miljenko ; Radojčić Badovinac, Anđelka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
European Journal of Human Genetics, vol 13 - suppl 1
/ - , 2005, 107-107
Skup
European Human Genetics Conference
Mjesto i datum
Prag, Češka Republika, 07.05.2005. - 10.05.2005
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Y chromosome microdeletions; chromosomal aberrations; male infertility
Sažetak
Microdeletions of the long arm of the chromosome Y and major chromosomal aberrations are common cause of male infertility. One hundred and twenty four infertile and fourty control fertile men from North-Adriatic part of Croatia were screened according to the Laboratory guidelines for molecular diagnosis of Y chromosome microdeletions. Microdeletions were determined in two patients in the nonobstructive azoospermia group (27 patients) making the frequency of 7, 4%. In the other investigated groups of patients: severe oligoasthenozoospermia (19), oligoasthenozoospermia (44) and normoasthenozoospermia (34) or in the control group, no microdeletions of the long arm of chromosome Y were found. Microdeletion found in one patient was spanning AZFb and AZFc regions, while in the other one was restricted to AZFc region. Cytogenetic analysis was made in 85 patients included in the microdeletion testing. The overall frequency of chromosomal aberrations was 4, 7%. Reciprocal translocation t(12, 22) was found in normoasthenozoospermic man (1, 2%), and Klinefelter syndrome was determined in three patients (3, 5%) with azoospermia. The frequency of Y chromosome microdeletions is within values reported by other authors.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Anđelka Radojčić Badovinac
(autor)
Alena Buretić-Tomljanović
(autor)
Ivan Vlastelić
(autor)
Jadranka Vraneković
(autor)
Saša Ostojić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE