A case report of necrotizing enterocolitis in a moderately preterm neonate with LCHADD-A call to focus on the basics while utilizing advanced new therapies

• Главные авторы: Marina Metzler (Автор), William Burns (Автор), Carly Mitchell (Автор), Stephanie Napolitano (Автор), Bimal P. Chaudhari (Автор)
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• Опубликовано: Frontiers Media S.A., 2023-02-01T00:00:00Z.
• Предметы: article
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Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is an autosomal recessive condition of impaired beta-oxidation. Traditionally, treatment included restriction of dietary long-chain fatty acids via a low-fat diet and supplementation of medium chain triglycerides. In 2020, triheptanoin r...