Genotype-phenotype associations in 90 children with congenital hyperinsulinism

Autor: Melikyan, M., Christesen, H., Petryakina, E., Tulpakov, A., Tihonovich, J., Stepanov, A., Kareva, M., Flanagan, S., Ellard, S., Brusgaard, K., Peterkova, V., Hussain, K.

Publikováno v: Melikyan, M, Christesen, H, Petryakina, E, Tulpakov, A, Tihonovich, J, Stepanov, A, Kareva, M, Flanagan, S, Ellard, S, Brusgaard, K, Peterkova, V & Hussain, K 2015, ' Genotype-phenotype associations in 90 children with congenital hyperinsulinism ', Hormone Research in Paediatrics, vol. 84, no. S1, P3-1063, pp. 504-505 . https://doi.org/10.1159/000437032

Background: Congenital hyperinsulinism (CHI) is a common cause of hypoglycaemia in neonates, infants and children. CHI is a heterogeneous disease in terms of clinical presentation, genetics and histology. Objective and hypotheses: The aim of this stu

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