prikaz prve stranice dokumenta An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome
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An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome
Journal of pediatric hematology/oncology, 40 (2018), 2; 127-128. https://doi.org/10.1097/MPH.0000000000001025
Butorac Ahel, Ivona; Baraba Dekanić, Kristina; Palčevski, Goran; Roganović, Jelena

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Butorac Ahel, I., Baraba Dekanić, K., Palčevski, G. i Roganović, J. (2018). An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome. Journal of pediatric hematology/oncology, 40. (2), 127-128. doi: 10.1097/MPH.0000000000001025

Butorac Ahel, Ivona, et al. "An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome." Journal of pediatric hematology/oncology, vol. 40, br. 2, 2018, str. 127-128. https://doi.org/10.1097/MPH.0000000000001025

Butorac Ahel, Ivona, Kristina Baraba Dekanić, Goran Palčevski i Jelena Roganović. "An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome." Journal of pediatric hematology/oncology 40, br. 2 (2018): 127-128. https://doi.org/10.1097/MPH.0000000000001025

Butorac Ahel, I., et al. (2018) 'An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome', Journal of pediatric hematology/oncology, 40(2), str. 127-128. doi: 10.1097/MPH.0000000000001025

Butorac Ahel I, Baraba Dekanić K, Palčevski G, Roganović J. An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome. Journal of pediatric hematology/oncology [Internet]. 2018. [pristupljeno 03.12.2024.];40(2):127-128. doi: 10.1097/MPH.0000000000001025

I. Butorac Ahel, K. Baraba Dekanić, G. Palčevski i J. Roganović, "An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome", Journal of pediatric hematology/oncology, vol. 40, br. 2, str. 127-128, 2018. [Online]. Dostupno na: https://urn.nsk.hr/urn:nbn:hr:184:924178. [Citirano: 03.12.2024.]

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Podaci o radu
Naslov (engleski)An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome
AutorIvona Butorac Ahel
MBZ: 334051
AutorKristina Baraba Dekanić
AutorGoran Palčevski
AutorJelena Roganović
Autorova ustanovaSveučilište u Rijeci
Medicinski fakultet
(Katedra za pedijatriju)
Znanstveno / umjetničko
područje, polje i grana		BIOMEDICINA I ZDRAVSTVO
Kliničke medicinske znanosti
Pedijatrija
Sažetak (engleski)
Hereditary spherocytosis is the most frequent congenital hemolytic anemia and is characterized with variable degree of anemia, jaundice, and splenomegaly. In the case of severe hyperbilirubinemia out of proportion with hemolysis, other causes of hyperbilirubinemia must be considered. Gilbert syndrome (GS) is an autosomal dominant disorder characterized with intermittent hyperbilirubinemia without any other sign and symptom of liver disease as a result of reduced activity of uridine diphosphate-glucuronyl transferase 1A1. The calculated rate of coexistence of these 2 diseases is 15 to 35/million births. Here we present a 21-month-old girl with hereditary spherocytosis diagnosed at the age of 40 days with hyperbilirubinemia out of proportion of hemolysis which led to diagnosis of GS. Thereby, the diagnosis of GS should be considered in unexplained unconjugated hyperbilirubinemia in different age groups, including infants and toddlers.
Ključne riječi (engleski)
Jezikengleski
Vrsta publikacijeZnanstveni rad - Prikaz slučaja
Status objaveObjavljen
Vrsta recenzijeRecenziran
Verzija publikacijeObjavljena verzija rada (izdavačev PDF)
Naslov časopisaJournal of pediatric hematology/oncology
Brojčani podacivol. 40, br. 2, str. 127-128
p-ISSN1077-4114
DOIhttps://doi.org/10.1097/MPH.0000000000001025
URN:NBNurn:nbn:hr:184:924178
Datum objave publikacije2018
URL dokumentahttp://bib.irb.hr/1023247
Vrsta resursaTekst
Prava pristupaOgraničen pristup
Uvjeti korištenjaIkona licence Zaštićeno autorskim pravom.
Datum i vrijeme pohrane2022-02-07 12:36:09