A Clinical and Genetic Evaluation of Cases with Folate Receptor α Gene Mutation: A Case Series from Türkiye
Akgun A, Tas I
Diagnostics · 2025
Key finding
Our study suggests that FOLR1-related CFD should be considered in cases with febrile convulsions, developmental delay, ataxia, autism spectrum disorder, acquired microcephaly, and MRI findings of white matter involvement and cerebellar atrophy.
- Condition
- ADHD
- Stimulation
- taVNS
- Evidence tier
- Case Report / Series
- Participants
- —
Cite this study
Akgun, A., & Tas, I. (2025). A Clinical and Genetic Evaluation of Cases with Folate Receptor α Gene Mutation: A Case Series from Türkiye. Diagnostics, 15(7), 892. https://doi.org/10.3390/diagnostics15070892
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