prikaz prve stranice dokumenta An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome
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Scientific paper - Case study
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. & 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, no. 2, 2018, pp. 127-128. https://doi.org/10.1097/MPH.0000000000001025

Butorac Ahel, Ivona, Kristina Baraba Dekanić, Goran Palčevski and Jelena Roganović. "An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome." Journal of pediatric hematology/oncology 40, no. 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), pp. 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 [cited 2024 July 08];40(2):127-128. doi: 10.1097/MPH.0000000000001025

I. Butorac Ahel, K. Baraba Dekanić, G. Palčevski and 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, no. 2, pp. 127-128, 2018. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:184:924178. [Accessed: 08 July 2024]

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Metadata
Title (english)An infant with unusually high unconjugated hyperbilirubinemia due to coexistence of hereditary spherocytosis and Gilbert syndrome
AuthorIvona Butorac Ahel
MBZ: 334051
AuthorKristina Baraba Dekanić
AuthorGoran Palčevski
AuthorJelena Roganović
Author's institutionUniversity of Rijeka
Faculty of Medicine
(Department of Pediatrics)
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Pediatrics
Abstract (english)
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.
Keywords (english)
Languageenglish
Publication typeScientific paper - Case study
Publication statusPublished
Peer reviewPeer review
Publication versionPublished version
Journal titleJournal of pediatric hematology/oncology
Numberingvol. 40, no. 2, pp. 127-128
p-ISSN1077-4114
DOIhttps://doi.org/10.1097/MPH.0000000000001025
URN:NBNurn:nbn:hr:184:924178
Publication2018
Document URLhttp://bib.irb.hr/1023247
Type of resourceText
Access conditionsRestricted access
Terms of useLicence In copyright icon
Created on2022-02-07 12:36:09