Severe galactosemia of type 1 in a premature baby: difficulties of differential diagnosis

Galactosemia is a hereditary disease characterized by impaired galactose metabolism. A newborn fed by breast milk or an adapted infant formula quickly develop clinical manifestations of the disease associated with accumulation of galactose and its toxic metabolites in the body. Neonatal screening is...

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Bibliografische gegevens
Hoofdauteurs: I. V. Nikitina, I. M. Amelin, I. Sh. Makhmudov, O. A. Krogh-Jensen, E. A. Tumasyan, А. A. Lenyushkina, A. V. Degtyareva, D. N. Degtyarev
Formaat: Artigo
Taal:Russo
Gepubliceerd in: Ltd. “The National Academy of Pediatric Science and Innovation” 2020-11-01
Reeks:Rossijskij Vestnik Perinatologii i Pediatrii
Onderwerpen:
children
preterm baby
galactosemia
neonatal screening
galactose
intensive care unit
Online toegang:https://www.ped-perinatology.ru/jour/article/view/1240
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