Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Late-onset MADD in Yemen caused by a novel ETFDH mutation misdiagnosed as ADEM.

Multiple sclerosis and related disorders - 1 Feb 2021

Lian Ling, Chen Dingbang, Li Jing, Tan Shuangquan, Que Jiali, Feng Huiyu, Fang Yannan, Chen Ling, Zhou Hongyan

Abstract excerpt

We report a case of late-onset multiple acyl-CoA dehydrogenase deficiency (MADD) with recurrent abdominal pain, vomiting, and impaired consciousness as the initial symptoms in Yemen; the case showed distinctive characteristics from those of Asian or Caucasian patients. Initially, he was misdiagnosed with pancreatitis, acute disseminated encephalomyelitis(ADEM), and fatty liver. Final diagnosis was further...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Diagnostic Errors
Share to Electron-Transferring Flavoproteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Guanine Nucleotide Exchange Factors

Share to Iron-Sulfur Proteins

Share to Middle East

Share to Multiple Acyl Coenzyme A Dehydrogenase Deficiency

Share to Oxidoreductases Acting on CH-NH Group Donors

Source

Identifiers

PMID: 33383363
DOI: 10.1016/j.msard.2020.102689

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Late-onset MADD in Yemen caused by a novel ETFDH mutation misdiagnosed as ADEM.PMID 33383363Read ↗

A systematic review of late-onset and very-late-onset multiple acyl-coenzyme A dehydrogenase deficiency: Cohort analysis and patient report from Taiwan.Semantic proximity Read ↗

An unusual presentation of type III late onset multiple-acyl-CoA dehydrogenase deficiency leading to a review of its classification system.Semantic proximity Read ↗

Late-onset multiple acyl-CoA dehydrogenase deficiency: an insidious presentation.Semantic proximity Read ↗

Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency.Semantic proximity Read ↗

[Analysis of clinical features and genetic variants in three children with late-onset Multiple acyl-Coenzyme A dehydrogenase deficiency].Semantic proximity Read ↗

Neonatal-onset multiple acyl-CoA dehydrogenase deficiency (MADD) in the ETFDH gene: A case report and a literature review.Semantic proximity Read ↗

Dihydrolipoamide Dehydrogenase (DLD) Deficiency: A Case ReportSemantic proximity Read ↗

Clinical characteristics and gene mutation analysis of an adult patient with ETFDH‑related multiple acyl‑CoA dehydrogenase deficiency.Semantic proximity Read ↗

A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiency.Semantic proximity Read ↗

Late-onset multiple acyl-CoA dehydrogenase deficiency: a frequently missed diagnosis?Semantic proximity Read ↗

Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.