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References: 1.<\/strong>Rocha JC, MacDonald A. Dietary intervention in the management of phenylketonuria: current perspectives. Pediatric Health Med<\/em> Ther<\/em>. 2016;7:155-163. 2.<\/strong> Vockley J, Andersson HC, Antshel KM, et al; American College of Medical Genetics and Genomics Therapeutic Committee. Phenylalanine hydroxylase deficiency: diagnosis and management guidelines. Genet Med<\/em>. 2014;16(2):188-200. 3.<\/strong> Rocha JC, Ahring KK, Ausel H, et al. Expert consensus on the long-term effectiveness of medical nutrition therapy and its impact on the outcomes of adults with phenylketonuria. Nutrients.<\/em> 2023;15(18):3940. 4.<\/strong> Lehman S. What to eat when you have PKU. Dietary recommendations for better management. Verywell Health.<\/em> Updated July 12, 2023. Accessed December 22, 2023. https:\/\/www.verywellhealth.com\/what-is-the-pku-diet-2507160. 5.<\/strong> van Wegberg AMJ, MacDonald A, Ahring K, et al. The complete European guidelines of phenylketonuria: diagnosis and treatment. Orphanet J Rare Dis.<\/em> 2017;12(1):162. 6.<\/strong> MacLeod EL, Ney DM. Nutritional management of phenylketonuria. Ann Nestle (Engl)<\/em> 2010;68:58-69. doi:10:1159\/00312813. 7.<\/strong> US Department of Agriculture. Agricultural Research Service\/Food Data Central\/Food Search. 8.<\/strong> Enns GM, Koch R, Brumm V, Blakely E, Suter R, Jurecki E. Suboptimal outcomes in patients with PKU treated early with diet alone: revisiting the evidence. Mol Genet Metab<\/em>. 2010;101(2-3):99-109. 9.<\/strong> Ford S, O\u2019Driscoll M, MacDonald A. Living with phenylketonuria: lessons from the PKU community. Mol Genet Metab Rep<\/em>. 2018;17:57-63. 10<\/strong>. van Spronsen FJ, van Wegberg AMJ, Ahring K, et al. Key European guidelines for the diagnosis and management of patients with phenylketonuria. Lancet Diabetes Endocrinol<\/em>. 2017;5(9):743-756. 11.<\/strong> Trefz FK, van Spronsen FJ, MacDonald A, et al. Management of adult patients with phenylketonuria survey results from 24 countries. Eur J Pediatr<\/em>. 2015;174(1):119-127. 12.<\/strong> Levy H, Lamppu D, Anastosoaie V, et al. 5-year retrospective analysis of patients with phenylketonuria (PKU) and hyperphenylalaninemia treated at two specialized clinics. Mol Genet Metab<\/em>. 2020;129(3):177-185. <\/small><\/p>\n <\/div>\n <\/div>\n <\/div>\n<\/div>","protected":false},"excerpt":{"rendered":"","protected":false},"author":3,"featured_media":0,"parent":272,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"inline_featured_image":false,"footnotes":""},"class_list":["post-371","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nPKU Phe-restricted Diet l Reduce Phe levels l Diet Challenges<\/title>\n\n\n\n\n\n\n\n\n\n\n\n