Neonatal haemochromatosis (Q86832): Difference between revisions
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A hemocromatose neonatal é um distúrbio de armazenamento de ferro de etiologia desconhecida, presente ao nascimento, e caracterizado pela associação de insuficiência hepatocelular grave com hiperbilirrubinemia, sinais de hemorragia, edema, ascite, hipoglicemia e acidose láctica com pouca ou sem elevação das transaminases. | |||
| description / en | description / en | ||
Neonatal hemochromatosis is an iron storage disorder of unknown etiology present at birth, and characterised by the association of severe hepatocellular failure with hyperbilirubinemia, signs of haemorrhage, oedema, ascites, hypoglycaemia, and lactic acidosis with little to no elevation of transaminases. | |||
Revision as of 12:23, 15 August 2026
Neonatal hemochromatosis is an iron storage disorder of unknown etiology present at birth, and characterised by the association of severe hepatocellular failure with hyperbilirubinemia, signs of haemorrhage, oedema, ascites, hypoglycaemia, and lactic acidosis with little to no elevation of transaminases.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1476368232 |
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| English | Neonatal haemochromatosis |
Neonatal hemochromatosis is an iron storage disorder of unknown etiology present at birth, and characterised by the association of severe hepatocellular failure with hyperbilirubinemia, signs of haemorrhage, oedema, ascites, hypoglycaemia, and lactic acidosis with little to no elevation of transaminases. |
