Management of pregnancy in a patient with long-chain 3-hydroxyacyl CoA dehydrogenase deficiency

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is a rare mitochondrial defect of β-oxidation of long-chain fatty acids. Patients may present with muscle pain, hypotonia, peripheral neuropathy, cardiomyopathy, recurrent rhabdomyolysis and sudden death. Dietary management of LCHADD aim...

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Bibliographic Details
Main Authors:	Donnelly, J.C (Author), Gillman, B. (Author), Ivory, J. (Author), McCarthy, C.M (Author), McNulty, J. (Author), O'Byrne, J.J (Author), Shakerdi, L.A (Author), Sheerin, A. (Author), Treacy, E.P (Author)
Format:	Article
Language:	English
Published:	John Wiley and Sons Inc 2022
Subjects:	acylcarnitine long-chain 3-hydroxyacyl CoA dehydrogenase deficiency pregnancy rhabdomyolysis
Online Access:	View Fulltext in Publisher

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Management of pregnancy in a patient with long-chain 3-hydroxyacyl CoA dehydrogenase deficiency

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