Evidence map›Paper›PMID 40192239›Full record

ReviewMolecular genetics & genomic medicine2025

Expanding the Clinical and Genetic Spectrum of Mitochondrial Short-Chain Enoyl-CoA Hydratase 1 Deficiency: Insights From Two Unrelated Chinese Families.

Jihua Wu, Xuehui Hu, Zhongli Zhao, Zhen Zhao, Bin Yang

Abstract readCase ReportsReview
In one paragraph

Review in Molecular genetics & genomic medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jihua WuDepartment of Neurology, Anhui Provincial Children's Hospital, Hefei, China.ORCID https://orcid.org/0009-0009-7375-8019
Xuehui HuDepartment of Neurology, Anhui Provincial Children's Hospital, Hefei, China.
Zhongli ZhaoDepartment of Neurology, Anhui Provincial Children's Hospital, Hefei, China.
Zhen ZhaoDepartment of Imaging, Anhui Provincial Children's Hospital, Hefei, China.
Bin YangDepartment of Neurology, Anhui Provincial Children's Hospital, Hefei, China.

Funding

the Natural Science Foundation of Anhui Province 2108085MH268
6 · The paper itself

Abstract

backgroundMitochondrial short-chain enoyl-CoA hydratase 1 deficiency (ECHS1D) is a rare autosomal recessive disorder affecting valine metabolism, with clinical severity ranging from neonatal death to survival into adulthood. Despite advances in understanding ECHS1D, the genetic basis remains underexplored, particularly in underrepresented populations.

methodsThis study aimed to investigate the clinical and genetic characteristics of ECHS1D in two unrelated Chinese families and identify novel pathogenic variants. Clinical and genetic data were collected, and whole-genome sequencing was performed to identify pathogenic variants in the ECHS1 gene.

resultsThe first proband, a 15-month-old girl, presented with developmental delays and metabolic acidosis, with an MRI revealing abnormal signals in the basal ganglia. The second proband, a 6.5-year-old girl with movement-induced dystonia, exhibited lethargy following recurrent fever and vomiting, with similar MRI findings. Genetic testing identified novel compound heterozygous variants: c.759_762del (p.Gly255Valfs*21) and c.489G>A (p.Pro163=) in Proband 1 and c.518C>T (p.Ala173Val) and c.244G>A (p.Val82Met) in Proband 2. The c.759_762del (p.Gly255Valfs21) variant, identified for the first time, likely results in severe symptoms due to a loss of normal function.

conclusionThese findings expand the ECHS1 mutational spectrum and emphasize the importance of genetic testing for early diagnosis and personalized management of ECHS1D. Interventions such as dietary valine restriction and the avoidance of triggering factors may improve clinical outcomes, while further research is needed to explore targeted therapeutic strategies.

Indexed as

Amino Acid Metabolism, Inborn ErrorsEnoyl-CoA HydrataseChildEast Asian PeopleFemaleHumansInfantMaleMutationPedigreePhenotypeECHS1 protein, humanEnoyl-CoA Hydratasedevelopmental delayECHS1 geneEnoyl‐CoA hydratasemetabolic acidosis

Identifiers

PMID40192239
PMCPMC11973933

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.