Newborn Screening of Primary Carnitine Deficiency: An Overview of Worldwide Practices and Pitfalls to Define an Algorithm before Expansion of Newborn Screening in France

Primary Carnitine Deficiency (PCD) is a fatty acid oxidation disorder that will be included in the expansion of the French newborn screening (NBS) program at the beginning of 2023. This disease is of high complexity to screen, due to its pathophysiology and wide clinical spectrum. To date, few count...

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Detalles Bibliográficos
Autores principales: Lefèvre, Charles R., Labarthe, François, Dufour, Diane, Moreau, Caroline, Faoucher, Marie, Rollier, Paul, Arnoux, Jean-Baptiste, Tardieu, Marine, Damaj, Léna, Bendavid, Claude, Dessein, Anne-Frédérique, Acquaviva-Bourdain, Cécile, Cheillan, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944086/
https://www.ncbi.nlm.nih.gov/pubmed/36810318
http://dx.doi.org/10.3390/ijns9010006

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9944086/
https://www.ncbi.nlm.nih.gov/pubmed/36810318
http://dx.doi.org/10.3390/ijns9010006

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