Congenital cytomegalovirus infection (Q45756): Difference between revisions
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Afecção que acomete recém-nascidos, causada por uma infecção intrauterina por citomegalovírus. Essa condição é caracterizada por icterícia, baixo peso ao nascer, esplenomegalia, hepatomegalia ou pneumonia, se os sintomas se desenvolverem logo após o nascimento, ou pode ser assintomática. Esta condição comumente se apresenta mais tardiamente na vida com perda de audição, perda de visão ou deficiências de desenvolvimento. A transmissão é por transmissão vertical. A confirmação é feita pela detecção de citomegalovírus na urina, saliva, sangue ou outros tecidos corporais do recém-nascido em até 2-3 semanas após o nascimento. | |||
| description / en | description / en | ||
A condition affecting neonates, caused by an infection with cytomegalovirus in utero. This condition is characterised by jaundice, low birth weight, splenomegaly, hepatomegaly, or pneumonia if symptoms develop shortly after birth, or may be asymptomatic. This condition commonly presents later in life with loss of hearing, loss of vision, or developmental disabilities. Transmission is by vertical transmission. Confirmation is by detection of cytomegalovirus in neonatal urine, saliva, blood, or other body tissues within 2-3 weeks of birth. | |||
Revision as of 13:57, 13 August 2026
A condition affecting neonates, caused by an infection with cytomegalovirus in utero. This condition is characterised by jaundice, low birth weight, splenomegaly, hepatomegaly, or pneumonia if symptoms develop shortly after birth, or may be asymptomatic. This condition commonly presents later in life with loss of hearing, loss of vision, or developmental disabilities. Transmission is by vertical transmission. Confirmation is by detection of cytomegalovirus in neonatal urine, saliva, blood, or other body tissues within 2-3 weeks of birth.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | KA62.3 |
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| English | Congenital cytomegalovirus infection |
A condition affecting neonates, caused by an infection with cytomegalovirus in utero. This condition is characterised by jaundice, low birth weight, splenomegaly, hepatomegaly, or pneumonia if symptoms develop shortly after birth, or may be asymptomatic. This condition commonly presents later in life with loss of hearing, loss of vision, or developmental disabilities. Transmission is by vertical transmission. Confirmation is by detection of cytomegalovirus in neonatal urine, saliva, blood, or other body tissues within 2-3 weeks of birth. |
