Case reports highlight seizure challenges in two individuals with ring chromosome 14 syndrome, indicating severe implications for management.
The article presents cases of epilepsy in two patients with a rare hereditary condition associated with a chromosomal mutation—deletion of chromosome 14. The presented clinical cases are of professional and scientific interest, as they relate to a rare neurological condition, with refractory epilepsy as the leading manifestation.
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Novikova et al. (2025) studied this question.
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