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

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...

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Detalles Bibliográficos
Autores principales: Metzler, Marina, Burns, William, Mitchell, Carly, Napolitano, Stephanie, Chaudhari, Bimal P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969157/
https://www.ncbi.nlm.nih.gov/pubmed/36861082
http://dx.doi.org/10.3389/fped.2023.1081802

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969157/
https://www.ncbi.nlm.nih.gov/pubmed/36861082
http://dx.doi.org/10.3389/fped.2023.1081802

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