Pregled bibliografske jedinice broj: 257419
The MECP2 gene mutation screening in Rett syndrome patients from Croatia
The MECP2 gene mutation screening in Rett syndrome patients from Croatia // Annals of the New York Academy of Sciences, 1091 (2006), 1 (Part B); 225-232 doi:10.1196/annals.1378.069 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 257419 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
The MECP2 gene mutation screening in Rett syndrome patients from Croatia
Autori
Matijević, Tanja ; Knežević, Jelena ; Barišić, Ingeborg ; Čulić, Vida ; Rešić, Biserka ; Pavelić, Jasminka
Izvornik
Annals of the New York Academy of Sciences (0077-8923) 1091
(2006), 1 (Part B);
225-232
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
MECP2 gene ; mutation ; Rett syndrome
Sažetak
Rett syndrome (RTT) is an X-linked dominant neurodevelopmental disorder almost exclusively affecting females and is usually sporadic. Mutations in MECP2 gene have been found in more than 80% of females with typical features of RTT. In this study, we analyzed 15 sporadic cases of RTT. In 7 of 15 patients (47%), we detected pathogenic mutations in the coding parts of MECP2 fourth exon. We found two missense (T158M, R133C), two nonsense (R168X, R270X), two frameshift mutations (P217fs and a double deletion of 28-bp at 1132-1159 and 10-bp at 1167-1176), and one in-frame deletion (L383_E392del10). To our knowledge, the last two mutations have not been reported yet. We also detected one previously described polymorphism (S194S). In conclusion, these results show that the fourth exon should be the first one analyzed because it harbors most of the known mutations. Moreover, mutation-negative cases should be further analyzed for gross rearrangements. This is the first study of its kind in Croatia and it enabled us to give the patients an early confirmation of RTT diagnosis.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
Napomena
Rad je prezentiran na skupovima:
a) Cell Signaling World 2006 : Signal Transduction Pathways as therapeutic targets, održanom od 25.-28.01.2006.g., Luxembourg, Luxembourg ; (poster) Knjiga sažetaka str. 548-548 ;
b) European Human Genetics Conference 2006, održanom 06.-09-05-2006, Amsterdam, Nizozemska ; (predavanje) zbornik u: European Journal of Human Genetics (ISSN 1018-4813) 14 (2006) (S) , str. 225-232 ;
c) Četvrti hrvatski kongres humane genetike s međunarodnim sudjelovanjem, održan od 18.-20.10.2007., Malinska, Hrvatska ; Knjiga sažetaka u: Paediatria Croatica 51 (2007) str. 148-148.
POVEZANOST RADA
Projekti:
0072165
0098092
0216011
MZOS-072-1083107-0365 - Istraživanje epidemiologijskih i genetičkih osnova prirođenih mana (Barišić, Ingeborg, MZOS ) ( CroRIS)
Ustanove:
Klinika za dječje bolesti Medicinskog fakulteta,
Institut "Ruđer Bošković", Zagreb
Profili:
Vida Čulić
(autor)
Biserka Rešić
(autor)
Ingeborg Barišić
(autor)
Jelena Knežević
(autor)
Jasminka Pavelić
(autor)
Tanja Matijević Glavan
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE