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Article

Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia.

European journal of pediatrics - 1 Sept 2021

Raicevic Maja, Milenkovic Tatjana, Hussain Khalid, Djordjevic Maja, Martic Jelena, Todorovic Sladjana, Mitrovic Katarina, Sarajlija Adrijan, Vukovic Rade

Abstract excerpt

Persistent hypoglycaemia in newborns and infants is most commonly caused by congenital hyperinsulinism (CHI). Most CHI studies report outcomes in children from both consanguineous and non-consanguineous families which can affect the phenotype-genotype analysis. The aim of this study was to analyze characteristics of patients with CHI in 21 non-consanguineous families from Serbia. This retrospective cohort study...

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Child, Preschool
Congenital Hyperinsulinism
Consanguinity
Hyperinsulinism
Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Infant, Newborn

Sulfonylurea Receptors

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PMID: 33770274
DOI: 10.1007/s00431-021-04051-w

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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