Pregled bibliografske jedinice broj: 513822
Determination of G-6-PD in infants with hyperbilirubinemia of undetermined etiology in the Republic of Macedonia, preliminary results
Determination of G-6-PD in infants with hyperbilirubinemia of undetermined etiology in the Republic of Macedonia, preliminary results // Early Human Development 2010, Vol 86, Supplement November. 2nd International Congress of UENPS 2010, Istanbul, Turkey.
Istanbul, Turska, 2010. str. 138-139 (poster, međunarodna recenzija, sažetak, stručni)
CROSBI ID: 513822 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Determination of G-6-PD in infants with hyperbilirubinemia of undetermined etiology in the Republic of Macedonia, preliminary results
Autori
Piperkova, Katica ; Papazovska Cherepnalkovski, Anet ; Gruev, Todor ; Krželj, Vjekoslav
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Early Human Development 2010, Vol 86, Supplement November. 2nd International Congress of UENPS 2010, Istanbul, Turkey.
/ - , 2010, 138-139
Skup
2nd International Congress of UENPS 2010, Istanbul, Turkey
Mjesto i datum
Istanbul, Turska, 14.11.2010. - 17.11.2010
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
G-6-PD deficiency; hyperbilirubinemia; Republic of Macedonia
Sažetak
Aim Approximately 200 milion people worldwidw are estimated to suffer from G-6-PD deficiency with a significant difference in the incidence rate, depending on the region where they live. In Macedonia the incidence of G-6-PD deficiency was estimated 6% among Roma male children, and 1 % among Macedonians. Infants with G6PD deficiency suffer from hyperbilirubinemia significantly more frequently than those in control groups. The screening method for G-6-PD deficiency used at our Clinic showed low level of detection. Aim of study was to introduce a new, more sensitive quantitative method for G-6-PD detection and evaluate the level of G-6-PD in a group of infants with indirect hyperbilirubinemia/and or prolonged jaundice of undetermined etiology. Materials and methods The studied group is part of a large national study underway on the incidence of G-6-PD deficiency among children with hyperbilirubinemia of undetermined etiology. A group of 30 infants that were hospitalized at the University Pediatric Clinic neonatal department was prospectively evaluated. The study involved a questionnaire, clinical examination of subjects and laboratory analyses. Inclusion criteria were: term newborns, excluded other determined causes of jaundice, serum biliruin level higher oh 257 umol/l ( 15 mg/dL) and/or prolonged jaundice after one month. A quantitative spectrophotometric method was used for G-6-PD detection. Results The study group included 17 (56, .%) boys and 13 (43.3%) girls with median age of 30 (19-42.5) days. The mean +/- SD of G-6-PD was 217.69 ( +/- 53.29) mU/mL and the median (interquartile range) serum levels of G-6-PD were (0.05-0.35) mU/mL in zhe studied group. Conclusion These are preliminary results of G-6-PD testing in Macedonian infants with jaundice. A larger group has to be evaluated in order to produce reference values for G-6-PD in neonates and infants from the Republic of Macedonia and to astimate the incidence rate of this enzyme deficiency.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
216-0000000-3464 - Genske, kliničke i populacijske osobitosti deficita G-6-PD u Hrvatskoj (Krželj, Vjekoslav, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Split
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