Unknown

Dataset Information

0

Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples from a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in Denmark.


ABSTRACT: 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 acylcarnitines in follow-up samples were normal, but reverted to diagnostic levels when the patient developed clinical symptoms at the age of 8 months. At that time, a diagnosis of CPT1A deficiency was confirmed by sequence analysis of the CPT1A gene revealing homozygosity for a novel c.167C>T variation in exon 3. Enzyme activity measurements showed a relatively mild enzyme defect with a decreased residual enzyme activity of 17-25%. We conclude that CPT1A gene testing and/or enzyme assay is mandatory to confirm an abnormal newborn screen suggesting CPT1A deficiency to avoid delayed diagnoses.

SUBMITTER: Borch L 

PROVIDER: S-EPMC3509854 | biostudies-literature | 2012

REPOSITORIES: biostudies-literature

altmetric image

Publications

Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples from a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in Denmark.

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]

Similar Datasets

| S-EPMC8261918 | biostudies-literature
| S-EPMC8048260 | biostudies-literature
| S-EPMC4991433 | biostudies-literature
| S-EPMC7286491 | biostudies-literature
| S-EPMC8087699 | biostudies-literature
| S-EPMC3854250 | biostudies-literature
| S-EPMC9867753 | biostudies-literature
| S-EPMC5438386 | biostudies-literature
| S-EPMC5847421 | biostudies-literature