Neonatal screening for hereditary tyrosinaemia: are we there yet?

Arch Dis Child. 2015 Aug;100(8):720-1. doi: 10.1136/archdischild-2015-308265. Epub 2015 May 8.

Authors

Nedim Hadžić¹, Roshni Vara²

Affiliations

¹ Paediatric Centre for Hepatology, Gastroenterology and Nutrition, King's College Hospital, London, UK.
² Metabolic Medicine, Evelina Children's Hospital, London, UK.

PMID: 25957320
DOI: 10.1136/archdischild-2015-308265

No abstract available

Keywords: Hepatology; Metabolic; Paediatric Practice.

Publication types

Editorial
Comment

MeSH terms

Cyclohexanones / therapeutic use*
Enzyme Inhibitors / therapeutic use*
Female
Humans
Male
Neonatal Screening*
Nitrobenzoates / therapeutic use*
Tyrosinemias / diagnosis*
Tyrosinemias / drug therapy*

Substances

Cyclohexanones
Enzyme Inhibitors
Nitrobenzoates
nitisinone