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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Long-term monitoring of fatty acid oxidation defects: results from a MetabERN survey

Fig. 1

A Overview of the qualification of the respondents showing the type of patients treated per centre. B Overview of the number of patients with each LCFAOD treated in the different centres. LCFAOD Long chain fatty acid oxidation defects, NBS Newborn screening, VLCADD Very long-chain acyl-CoA dehydrogenase deficiency, CPT2D Carnitine palmitoyltransferase 2 deficiency, LCHADD Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency, MTPD Mitochondrial trifunctional protein deficiency

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