Ontology highlight
ABSTRACT:
SUBMITTER: Borch L
PROVIDER: S-EPMC3509854 | biostudies-literature | 2012
REPOSITORIES: biostudies-literature
Borch Luise L Lund Allan Meldgaard AM Wibrand Flemming F Christensen Ernst E Søndergaard Charlotte C Gahrn Birthe B Hougaard David Michael DM Andresen Brage Storstein BS Gregersen Niels N Olsen Rikke Katrine Jentoft RK
JIMD reports 20110922
Carnitine palmitoyl transferase (CPT) 1 A deficiency is a rare disorder of hepatic long-chain fatty acid oxidation. CPT1 deficiency is included in newborn screening programs in a number of countries to allow presymptomatic detection and early treatment of affected patients.We present a case of presymptomatic CPT1A deficiency detected through newborn screening in Denmark with diagnostic levels of carnitine and acylcarnitines in the initial dried blood spot. Levels of plasma-free carnitine and acy ...[more]