1. Introduction 1.1 Background of Encephalopathic Epilepsy 1.2 Importance of Genetic Research 1.3 Objectives of the Study 2. Literature Review 2.1 Overview of Pediatric Epilepsy 2.2 Genetic Factors in Epilepsy 2.3 KCNB1 Gene: Structure and Function 3. Methodology 3.1 Study Design 3.2 Participant Selection Criteria 3.3 Data Collection Methods 3.4 Statistical Analysis 4. The KCNB1 Gene 4.1 Gene Location and Expression 4.2 Mutations Linked to Epilepsy 4.3 Previous Studies and Findings 5. Clinical Manifestations 5.1 Symptoms of Encephalopathic Epilepsy 5.2 Impact on Sleep Patterns 5.3 Case Studies and Documented Evidence 6. Results 6.1 Genetic Mutation Data 6.2 Correlation with Sleep Disruption 6.3 Impact on Cognitive Development 7. Discussion 7.1 Interpretation of Findings 7.2 Gene and Phenotype Correlation 7.3 Implications for Treatment and Management 8. Conclusion and Future Directions 8.1 Summary of Key Findings 8.2 Limitations of the Study 8.3 Recommendations for Future Research
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