Pregled bibliografske jedinice broj: 318431
A possible autosomal dominant trait of familial recurrent spontaneous abortions and defective reproductive fitness
A possible autosomal dominant trait of familial recurrent spontaneous abortions and defective reproductive fitness // Periodicum Biologorum, Vol. 96 (3) / Silobrčić, Vlatko (ur.).
Zagreb: Hrvatsko prirodoslovno društvo, 1994. str. 256-256 (predavanje, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 318431 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
A possible autosomal dominant trait of familial recurrent spontaneous abortions and defective reproductive fitness
Autori
Radojčić, Anđelka ; Buretić-Tomljanović, Alena ; Vlastelić, Ivan ; Randić, Ljiljana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Periodicum Biologorum, Vol. 96 (3)
/ Silobrčić, Vlatko - Zagreb : Hrvatsko prirodoslovno društvo, 1994, 256-256
Skup
MECHANISMS IN LOCAL IMMUNITY, 2nd Alps-Adria Immunology and Allergology Meeting
Mjesto i datum
Opatija, Hrvatska, 26.09.1994. - 28.09.1994
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
recurrent spontaneous abortions; autosomal dominant trait
Sažetak
It has been postulated and experimentally supported that some idiopathic recurrent spontaneous abortions are caused by recessive lethal genes, probably linked to the major histocompatibility complex. The biggest problem in a trait analysis of some hereditary phenotypic characteristic or disease is genetical heterogeneity. The other problem is a possibility that the predisposition for disease is autosomal dominant characteristic, although disease is caused by recessive genes. In order to investigate genetics of idiopathic recurrent spontaneous abortions and defective reproductive fitness as a separated and unique clinical and immunologycal entity, 122 couples with two or less (44 couples), three or more (19) spontaneous abortions, blighted ovum or missed abortion (14), malformed child with or without spontaneous abortion (32) and sterility (13), were cytogenetically and genetically analysed. All gynaecological and hormonal causes are ruled out previously. Overall frequency of major chromosomal aberration is 13.1% (16/122) and 18% (22/122) for the chromosomal variants. Although, it is not still clear if the chromosomal variants or duplication of heterochromatin can interfere with reproductive fitness, those couples are also excluded because the content of heterochromatin of couples with malformed child with or without spontaneous abortion is significantly higher than in the control group (9 couples with one or more children and with no history of sp.ab.). The family pedigree of couples with familial spontaneous abortion shows vertical, no sex-related expression through several generation and no consanguinity, what leads us to conclusion that idiopathic recurrent spontaneous abortion or its predisposition has autosomal dominant trait. The next step will be to see if those genes are HLA-related or not.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
3-01-427
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Ljiljana Randić
(autor)
Anđelka Radojčić Badovinac
(autor)
Alena Buretić-Tomljanović
(autor)
Ivan Vlastelić
(autor)
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Časopis indeksira:
- Scopus