Normal neuroimaging in an infant with SUCLA2-related mitochondrial DNA depletion syndrome type 5: a case report of likely pathogenic variant.

Alsadi MO, Heikal Y, Al-Hasani F, Al Khasawneh D, Nasab A, Hrizat H, Almoustafa F, Hussain B

Open source

DOI
10.1093/omcr/omag172
Published
2026 Sep
Container
Oxford medical case reports
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1093/omcr/omag172,
  title = {Normal neuroimaging in an infant with SUCLA2-related mitochondrial DNA depletion syndrome type 5: a case report of likely pathogenic variant.},
  author = {Alsadi MO and Heikal Y and Al-Hasani F and Al Khasawneh D and Nasab A and Hrizat H and Almoustafa F and Hussain B},
  year = {2026},
  journal = {Oxford medical case reports},
  doi = {10.1093/omcr/omag172},
  url = {https://doi.org/10.1093/omcr/omag172}
}

RIS

TY  - JOUR
TI  - Normal neuroimaging in an infant with SUCLA2-related mitochondrial DNA depletion syndrome type 5: a case report of likely pathogenic variant.
AU  - Alsadi MO
AU  - Heikal Y
AU  - Al-Hasani F
AU  - Al Khasawneh D
AU  - Nasab A
AU  - Hrizat H
AU  - Almoustafa F
AU  - Hussain B
PY  - 2026
JO  - Oxford medical case reports
DO  - 10.1093/omcr/omag172
UR  - https://doi.org/10.1093/omcr/omag172
ER  - 

APA

MO, A., Y, H., F, A., D, A. K., A, N., H, H., F, A., & B, H. (2026). Normal neuroimaging in an infant with SUCLA2-related mitochondrial DNA depletion syndrome type 5: a case report of likely pathogenic variant.. Oxford medical case reports. https://doi.org/10.1093/omcr/omag172

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