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- Original (As adopted by EU)
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This is the original version as it was originally adopted in the EU.
This legislation may since have been updated - see the latest available (revised) version
Any infant < 2 years of age with at least one of the following 10:
Hepatospenomegaly
Mucocutaneous lesions
Condyloma lata
Persistent rhinitis
Jaundice
Pseudoparalysis (due to periostitis and osteochondritis)
Central nervous involvement
Anaemia
Nephrotic syndrome
Malnutrition
Laboratory criteria for case confirmation
At least one of the following three:
Demonstration of Treponema pallidum by dark field microscopy in the umbilical cord, the placenta, a nasal discharge or skin lesion material
Demonstration of Treponema pallidum by DFA-TP in the umbilical cord, the placenta, a nasal discharge or skin lesion material
Detection of Treponema pallidum — specific IgM (FTA-abs, EIA)
AND a reactive non-treponemal test (VDRL, RPR) in the child’s serum
Laboratory criteria for a probable case
At least one of the following three:
Reactive VDRL-CSF test result
Reactive non-treponemal and treponemal serologic tests in the mother’s serum
Infant’s non-treponemal antibody titre is four-fold or greater than the antibody titre in the mother’s serum
Any infant with an epidemiological link by human to human transmission (vertical transmission)
Any infant or child meeting the clinical criteria and with at least one of the following two:
An epidemiological link
Meeting the laboratory criteria for a probable case
Any infant meeting the laboratory criteria for case confirmation
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