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Clinical, pathological and genetic features and follow-up of 110 patients with late-onset MADD: a single-center retrospective study.

Human molecular genetics - 31 Mar 2022

Wen Bing, Tang Shuyao, Lv Xiaoqing, Li Duoling, Xu Jingwen, Olsen Rikke Katrine Jentoft, Zhao Yuying, Li Wei, Wang Tan, Shao Kai, Zhao Dandan, Yan Chuanzhu

Abstract excerpt

To observe a long-term prognosis in late-onset multiple acyl-coenzyme-A dehydrogenation deficiency (MADD) patients and to determine whether riboflavin should be administrated in the long-term and high-dosage manner, we studied the clinical, pathological and genetic features of 110 patients with late-onset MADD in a single neuromuscular center. The plasma riboflavin levels and a long-term follow-up study were...

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Share to Acyl Coenzyme A
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Guanine Nucleotide Exchange Factors

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Identifiers

PMID: 34718578
DOI: 10.1093/hmg/ddab308

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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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