Proposal for an individualized dietary strategy in patients with very long‐chain acyl‐CoA dehydrogenase deficiency

Author:

Bleeker Jeannette C.123,Kok Irene L.14,Ferdinandusse Sacha2,de Vries Maaike5,Derks Terry G.J.6,Mulder Margot F.7,Williams Monique8,Gozalbo Estela Rubio9,Bosch Annet M.3,van den Hurk Dorine T.4,de Sain‐van der Velden Monique G.M.10,Waterham Hans R.2,Wijburg Frits A.3,Visser Gepke13

Affiliation:

1. Department of Metabolic Diseases, Dutch Fatty Acid Oxidation Expertise CenterWilhelmina Children’s Hospital (UMCU), University Medical Center Utrecht, Internal Mail KE 04.306.0, PO Box 85090 3508 AB Utrecht Netherlands

2. Laboratory Genetic Metabolic DiseasesAcademic Medical Center Amsterdam Netherlands

3. Department of Pediatrics, Academic Medical CenterUniversity of Amsterdam Amsterdam Netherlands

4. Department of Internal Medicine and Dermatology, DieteticsUniversity Medical Center Utrecht Utrecht Netherlands

5. Department of PediatricsRadboud University Medical Center Nijmegen Netherlands

6. Department of Metabolic DiseasesBeatrix Children’s Hospital, University Medical Center Groningen Groningen Netherlands

7. Department of PediatricsVU University Medical Center Amsterdam Amsterdam Netherlands

8. Department of PediatricsErasmus MC‐Sophia Rotterdam Netherlands

9. Department of Pediatrics and Laboratory Genetic Metabolic DiseasesMaastricht University Medical Center Maastricht Netherlands

10. Department of Medical Genetics, Section Metabolic DiagnosticsWilhelmina Children’s Hospital, University Medical Center Utrecht Utrecht Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

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