Outcome of children with hereditary tyrosinaemia following newborn screening

Conclusions
Universal NBS for HT1 should be introduced in the UK.

Source: Archives of Disease in Childhood - July 17, 2015 Category: Pediatrics Authors: McKiernan, P. J., Preece, M. A., Chakrapani, A. Tags: Liver disease, Oncology, Immunology (including allergy), Child health, Disability, Screening (epidemiology), Artificial and donated transplantation, Metabolic disorders, Screening (public health) Original article Source Type: research