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. 2021 Feb 22;9:635353. doi: 10.3389/fped.2021.635353

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Copyright © 2021 Jansen, Klein, Buitenhuis, Rodenburg and Cornel.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Stakeholders involved and agenda with discussion points. Per condition relevant changes were made to the composition of the group, for example including a metabolic paediatrician or a neuromuscular paediatrician. ALD, X-linked adrenoleukodystrophy; BKT, methyl-acetoacetyl-CoA thiolase deficiency, ketothiolase deficiency; CACT, carnitine-acylcarnitine translocase deficiency; CPT1, carnitine palmitoyltransferase deficiency type 1; CPT2, carnitine palmitoyltransferase deficiency type 2; GALK, galactokinase deficiency; GAMT, guanidinoacetate methyltransferase deficiency; MMA, methylmalonic acidemia; MPS I, mucopolysaccharidosis type 1; PA, propionic acidemia; OCTN2, organic cation transporter 2 deficiency; RIVM, National Institute for Public Health and the Environment.