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Article

Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiency.

Neuromuscular disorders : NMD - 1 Feb 2016

Wang Zhaoxia, Hong Daojun, Zhang Wei, Li Wurong, Shi Xin, Zhao Danhua, Yang Xu, Lv He, Yuan Yun

Abstract excerpt

Multiple Acyl-CoA dehydrogenase deficiency (MADD) is an autosomal recessive disorder of fatty acid oxidation. Most patients with late-onset MADD are clinically characterized by lipid storage myopathy with dramatic responsiveness to riboflavin treatment. Abnormalities of peripheral neuropathy have rarely been reported in patients with late-onset MADD. We describe six patients who presented with proximal limb...

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Source

Identifiers

PMID: 26821934
DOI: 10.1016/j.nmd.2015.12.002

Genes

MADD
ETFDH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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