ArticleCureus2026
Clinical and Evolutionary Aspects of CDKL5-Related Developmental Epileptic Encephalopathy: A Case Report.
Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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0 citing papers in PubMed.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Cyclin-Dependent Kinase-Like 5 (CDKL5) Deficiency Disorder (CDD) is a rare genetic condition characterized by early-onset, pharmacoresistant epilepsy and severe global developmental delay. We report the case of a five-month-old infant who developed epileptic spasms at three months of age. Despite multiple antiepileptic therapies, seizures remained refractory. The clinical course was marked by persistent daily seizures and profound neurodevelopmental impairment. Genetic testing confirmed a pathogenic mutation in the
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Registered trials
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