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.
Authors
- Shimpei Matsuda
- Hiromichi Shoji (ORCID: https://orcid.org/0000-0003-2532-8910)
- Atsushi Yamashita (ORCID: https://orcid.org/0000-0002-2544-2134)
- Takato Akiba (ORCID: https://orcid.org/0009-0002-8507-2558)
- Yosuke Baba (ORCID: https://orcid.org/0000-0002-6861-1559)
- Shino Shimada (ORCID: https://orcid.org/0000-0001-5525-7362)
- Yasushi Okazaki (ORCID: https://orcid.org/0000-0003-3241-5502)
- Kei Murayama (ORCID: https://orcid.org/0000-0002-3923-8636)
- Shoji Ishida
Institutions
- Juntendo University (JP)
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
- 0.00