Pretražite po imenu i prezimenu autora, mentora, urednika, prevoditelja

Napredna pretraga

Pregled bibliografske jedinice broj: 1031672

Incidence of the 35delG/GJB2 mutation in low-risk newborns


Zaputovic, Sanja; Stanojevic, Milan; Medica, Igor; Peterlin, Borut; Petrovic, Oleg
Incidence of the 35delG/GJB2 mutation in low-risk newborns // The Journal of Maternal-Fetal & Neonatal Medicine, 21 (2008), 7; 463-468 doi:10.1080/14767050802123975 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 1031672 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Incidence of the 35delG/GJB2 mutation in low-risk newborns

Autori
Zaputovic, Sanja ; Stanojevic, Milan ; Medica, Igor ; Peterlin, Borut ; Petrovic, Oleg

Izvornik
The Journal of Maternal-Fetal & Neonatal Medicine (1476-7058) 21 (2008), 7; 463-468

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
neonates ; universal hearing screening ; otoacoustic emission ; auditory brainstem response ; genetic deafness ; 35delG/GJB2 mutation

Sažetak
Objective. To investigate, in a prospective study, the incidence of homozygotes and heterozygotes of the 35delG/GJB2 mutation for connexin 26 in the low-risk population of newborns undergoing two-stage universal neonatal hearing screening (UNHS). Patients and methods. The study population consisted of 1048 neonates born at the Department of Obstetrics and Gynecology, Rijeka University Hospital, Croatia, in the period between March 1, 2005 and June 30, 2005. The neonates underwent a two-stage UNHS program that included evoked otoacoustic emission (E-OAE) in all infants and automated auditory brainstem response (A-ABR) in those who did not pass the E-OAE. The 35delG/GJB2 mutation was determined in the umbilical cord blood of all examinees. Results. Fifteen out of 1048 infants (14.3 per 1000) did not pass the E-OAE, of whom three (2.86 per 1000) did not pass the A-ABR (two unilateral, one bilateral). The 35delG/GJB2 mutation was found in 13 out of 1033 infants who did pass the E-OAE and in one who did not pass the E- OAE. Thirteen out of 14 infants were heterozygotes (12.4 per 1000) and one infant was homozygote (0.95 per 1000) for the 35delG/GJB2 mutation. The homozygous infant had a bilateral pathological result on E-OAE and A- ABR, while 13 infants who were homozygotes passed the E-OAE. Conclusion. In all neonates, regardless of hearing impairment, genetic testing for the 35delG/GJB2 mutation is desirable in southern Croatia. The incidence of affected homozygous and healthy heterozygous transmitters of the 35delG/GJB2 mutation was in concordance with findings in southern European countries.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti



POVEZANOST RADA


Ustanove:
Medicinski fakultet, Rijeka,
Klinički bolnički centar Rijeka

Profili:

Avatar Url Oleg Petrović (autor)

Avatar Url Igor Medica (autor)

Avatar Url Milan Stanojević (autor)

Poveznice na cjeloviti tekst rada:

doi

Citiraj ovu publikaciju:

Zaputovic, Sanja; Stanojevic, Milan; Medica, Igor; Peterlin, Borut; Petrovic, Oleg
Incidence of the 35delG/GJB2 mutation in low-risk newborns // The Journal of Maternal-Fetal & Neonatal Medicine, 21 (2008), 7; 463-468 doi:10.1080/14767050802123975 (međunarodna recenzija, članak, znanstveni)
Zaputovic, S., Stanojevic, M., Medica, I., Peterlin, B. & Petrovic, O. (2008) Incidence of the 35delG/GJB2 mutation in low-risk newborns. The Journal of Maternal-Fetal & Neonatal Medicine, 21 (7), 463-468 doi:10.1080/14767050802123975.
@article{article, author = {Zaputovic, Sanja and Stanojevic, Milan and Medica, Igor and Peterlin, Borut and Petrovic, Oleg}, year = {2008}, pages = {463-468}, DOI = {10.1080/14767050802123975}, keywords = {neonates, universal hearing screening, otoacoustic emission, auditory brainstem response, genetic deafness, 35delG/GJB2 mutation}, journal = {The Journal of Maternal-Fetal and Neonatal Medicine}, doi = {10.1080/14767050802123975}, volume = {21}, number = {7}, issn = {1476-7058}, title = {Incidence of the 35delG/GJB2 mutation in low-risk newborns}, keyword = {neonates, universal hearing screening, otoacoustic emission, auditory brainstem response, genetic deafness, 35delG/GJB2 mutation} }
@article{article, author = {Zaputovic, Sanja and Stanojevic, Milan and Medica, Igor and Peterlin, Borut and Petrovic, Oleg}, year = {2008}, pages = {463-468}, DOI = {10.1080/14767050802123975}, keywords = {neonates, universal hearing screening, otoacoustic emission, auditory brainstem response, genetic deafness, 35delG/GJB2 mutation}, journal = {The Journal of Maternal-Fetal and Neonatal Medicine}, doi = {10.1080/14767050802123975}, volume = {21}, number = {7}, issn = {1476-7058}, title = {Incidence of the 35delG/GJB2 mutation in low-risk newborns}, keyword = {neonates, universal hearing screening, otoacoustic emission, auditory brainstem response, genetic deafness, 35delG/GJB2 mutation} }

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


Citati:





    Contrast
    Increase Font
    Decrease Font
    Dyslexic Font