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<p>This article presents two cases of epilepsy in patients with a rare hereditary pathology associated with a chromosomal mutation – deletion of chromosome 14. The clinical observations described here are of practical and scientific interest, as they relate to a rare neurological pathology where resistant epilepsy is the leading manifestation.</p>

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Ring Chromosome 14 Syndrome

  • 期刊论文

  • 发表日期：

    2026年3月27日

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  • L. B. Novikova,
  • N. M. Fayzullina,
  • A. P. Akopyan,
  • K. M. Ziultsle

摘要

This article presents two cases of epilepsy in patients with a rare hereditary pathology associated with a chromosomal mutation – deletion of chromosome 14. The clinical observations described here are of practical and scientific interest, as they relate to a rare neurological pathology where resistant epilepsy is the leading manifestation.