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July 10, 2024

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

Mengqin Wang Xi Wang Ang Ma Yu Gu Xiaotong Zhao Yaodong Zhang Dongxiao Li Yongxing Chen Haiyan Wei

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Abstract

To explore the clinical characteristics and genetic variants in three children with late-onset Multiple acyl-Coenzyme A dehydrogenase deficiency (MADD type Ⅲ).

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Cite This Study

Wang et al. (2024) studied this question.

synapsesocial.com/papers/68e60bfeb6db64358759f957 https://doi.org/10.3760/cma.j.cn511374-20230611-00355

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency (MADD): Clinical Features, Diagnostic Challenges, and the Role of Oxidative Stress in Pathophysiology2025 · 2 citations
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3Deep Intronic ETFDH Variants Represent a Recurrent Pathogenic Event in Multiple Acyl-CoA Dehydrogenase Deficiency2024 · 7 citations
4Sensory neuropathy as a manifestation of multiple acyl-coenzyme A dehydrogenase deficiency2024 · 4 citations
5[Clinical and genetic features of children with 3-methylcrotonyl-coenzyme A carboxylase deficiency: an analysis of six cases].2024