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dc.contributor.authorRocha, Carolina Roos Mariano dapt_BR
dc.contributor.authorGuedes, Renata Rostirolapt_BR
dc.contributor.authorKieling, Carlos Oscarpt_BR
dc.contributor.authorAdami, Marina Rossatopt_BR
dc.contributor.authorCerski, Carlos Thadeu Schmidtpt_BR
dc.contributor.authorVieira, Sandra Maria Gonçalvespt_BR
dc.date.accessioned2018-07-10T02:32:54Zpt_BR
dc.date.issued2017pt_BR
dc.identifier.issn2090-6811pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/180266pt_BR
dc.description.abstractNeonatal liver failure (NLF) is amajor cause of neonatalmorbidity andmortality, presenting as acute liver failure and/or congenital cirrhosis. Many affected patients show antenatal signs of fetal injury. There are several causes of NLF and early diagnosis is mandatory to elucidate the etiology and determine a specific treatment or the best management strategy. Gestational alloimmune liver disease associated with neonatal hemochromatosis (GALD-NH) is a rare but potentially treatable cause of NLF. It should be considered in any neonate with fetal signs of disease and postnatal signs of liver failure with no other identifiable causes. GALD-NH is often diagnosed late and patients are therefore referred late to specialized centers, delaying treatment. This case highlights the consequences of late diagnosis and treatment of GALD-NH and emphasizes the importance of a high grade of suspicion of this disease in order to refer the patient to a specialized center soon enough to perform the appropriate treatment.en
dc.format.mimetypeapplication/pdf
dc.language.isoengpt_BR
dc.relation.ispartofCase reports in pediatrics. New York. Vol. 2017 (2017), 7432859, 7 p.pt_BR
dc.rightsOpen Accessen
dc.subjectFalência hepáticapt_BR
dc.subjectRecém-nascidopt_BR
dc.subjectHemocromatosept_BR
dc.titleNeonatal liver failure and congenital cirrhosis due to gestational alloimmune liver disease : a case report and literature reviewpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001070482pt_BR
dc.type.originEstrangeiropt_BR


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