Congenital viral hepatitis (Q45758): Difference between revisions

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Doença do fígado acometendo o recém-nascido, causada por uma infecção intrauterina pelo vírus da hepatite A, B, C, D ou E. Esta doença é caracterizada por letargia, icterícia, distensão abdominal, prejuízo no crescimento ou fezes esbranquiçadas. A transmissão ocorre por exposição vertical. A confirmação é feita pela identificação do vírus da hepatite A, B, C, D ou E em uma amostra de sangue do recém-nascido.
description / endescription / en
 
A disease of the liver affecting the neonate, caused by an infection with either hepatitis A, B, C, D, or E virus in utero. This disease is characterised by lethargy, jaundice, abdominal distention, failure to thrive, or clay coloured stools. Transmission is by vertical transmission. Confirmation is by identification of the hepatitis A, B, C, D, or E virus in a blood sample from the neonate.

Revision as of 13:57, 13 August 2026

A disease of the liver affecting the neonate, caused by an infection with either hepatitis A, B, C, D, or E virus in utero. This disease is characterised by lethargy, jaundice, abdominal distention, failure to thrive, or clay coloured stools. Transmission is by vertical transmission. Confirmation is by identification of the hepatitis A, B, C, D, or E virus in a blood sample from the neonate.
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KA62.9
    English
    Congenital viral hepatitis
    A disease of the liver affecting the neonate, caused by an infection with either hepatitis A, B, C, D, or E virus in utero. This disease is characterised by lethargy, jaundice, abdominal distention, failure to thrive, or clay coloured stools. Transmission is by vertical transmission. Confirmation is by identification of the hepatitis A, B, C, D, or E virus in a blood sample from the neonate.

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