Evaluation of earlier versus later dietary management in long-chain 3-hydroxyacyl-CoA dehydrogenase or mitochondrial trifunctional protein deficiency: a systematic review

BACKGROUND: Mitochondrial trifunctional protein (MTP) and long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencies are rare fatty acid β-oxidation disorders. Without dietary management the conditions are life-threatening. We conducted a systematic review to investigate whether pre-symptomatic...

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Dades bibliogràfiques
Publicat a:Orphanet J Rare Dis
Autors principals: Fraser, Hannah, Geppert, Julia, Johnson, Rebecca, Johnson, Samantha, Connock, Martin, Clarke, Aileen, Taylor-Phillips, Sian, Stinton, Chris
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2019
Matèries:
Review
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6858661/
https://ncbi.nlm.nih.gov/pubmed/31730477
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-019-1226-y
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