Siblings of FBXL4-related mitochondrial DNA depletion syndrome, leading to fatal fulminant pneumonia

The F-box and leucine-rich repeat protein 4 (<i>FBXL4</i>) is a nuclear encoded mitochondrial protein essential for mitochondrial DNA (mtDNA) maintenance. Biallelic variants in <i>FBXL4</i> cause FBXL4-related mitochondrial DNA depletion syndrome (FBXL4-MTDPS), characterized by lactic acidosis and developmental delay. We report two siblings diagnosed with FBXL4-MTDPS who died of fulminant pneumonia in infancy; autopsy revealed extensive pulmonary inflammation consistent with severe bacterial infection. FBXL4-MTDPS may involve intrinsic defects in pulmonary infection defense, increasing susceptibility to fatal infection such as pneumonia.

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Publication Details

Journal
Molecular Genetics and Metabolism Reports
Published
2025-10-11
DOI
https://doi.org/10.1016/j.ymgmr.2025.101266
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
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article

Siblings of FBXL4-related mitochondrial DNA depletion syndrome, leading to fatal fulminant pneumonia

Shimpei Matsuda, Hiromichi Shoji, Atsushi Yamashita, Takato Akiba et al.
Molecular Genetics and Metabolism Reports
Mitochondrial Function and Pathology
article

Siblings of FBXL4-related mitochondrial DNA depletion syndrome, leading to fatal fulminant pneumonia

Shimpei Matsuda, Hiromichi Shoji, Atsushi Yamashita, Takato Akiba, Yosuke Baba, Shino Shimada, Yasushi Okazaki, Kei Murayama, Shoji Ishida
article en

Abstract

The F-box and leucine-rich repeat protein 4 (<i>FBXL4</i>) is a nuclear encoded mitochondrial protein essential for mitochondrial DNA (mtDNA) maintenance. Biallelic variants in <i>FBXL4</i> cause FBXL4-related mitochondrial DNA depletion syndrome (FBXL4-MTDPS), characterized by lactic acidosis and developmental delay. We report two siblings diagnosed with FBXL4-MTDPS who died of fulminant pneumonia in infancy; autopsy revealed extensive pulmonary inflammation consistent with severe bacterial infection. FBXL4-MTDPS may involve intrinsic defects in pulmonary infection defense, increasing susceptibility to fatal infection such as pneumonia.

Molecular Genetics and Metabolism ReportsVol. 45
Juntendo University (JP)
Openalex Percentile: Top 72%
Mitochondrial Function and Pathology
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Siblings of FBXL4-related mitochondrial DNA depletion syndrome, leading to fatal fulminant pneumonia — Shimpei Matsuda, Hiromichi Shoji, et al. · Molecular Genetics and Metabolism Reports (2025) | TGRS Research Map | TGRS