Sensory neuropathy as a manifestation of multiple acyl-coenzyme A dehydrogenase deficiency.
Lipid disorders
Metabolic disorders
Neuro genetics
Neurology
Neuromuscular disease
Journal
BMJ case reports
ISSN: 1757-790X
Titre abrégé: BMJ Case Rep
Pays: England
ID NLM: 101526291
Informations de publication
Date de publication:
15 Mar 2024
15 Mar 2024
Historique:
medline:
18
3
2024
pubmed:
16
3
2024
entrez:
15
3
2024
Statut:
epublish
Résumé
Multiple acyl-coenzyme A dehydrogenase deficiency (MADD) is a rare metabolic disorder which typically manifests with muscle weakness. However, despite late-onset MADD being treatable, it is often misdiagnosed, due in part to the heterogeneity of presentations. We report a case of late-onset MADD manifesting first as a sensory neuropathy before progressing to myopathic symptoms and acute metabolic decompensation. Early diagnostic workup with acylcarnitine profiling and organic acid analysis was critical in patient outcome; metabolic decompensation and myopathic symptoms were completely reversed with riboflavin supplementation and dietary modification, although sensory neuropathy persisted. Clinical consideration of MADD as part of the differential diagnosis of neuropathy with myopathy is crucial for a timely diagnosis and treatment of MADD.
Identifiants
pubmed: 38490702
pii: 17/3/e259192
doi: 10.1136/bcr-2023-259192
pii:
doi:
Substances chimiques
Acyl-CoA Dehydrogenase
EC 1.3.8.7
Electron-Transferring Flavoproteins
0
Riboflavin
TLM2976OFR
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© BMJ Publishing Group Limited 2024. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.