A 4-Year-Old Bahraini Girl With Developmental Delay and Epilepsy of Infancy With Migrating Focal Seizures Associated With KCNT1 Gene Mutation

Noora Ebrahim AlHadi; Hessa Mohammed Albuainain; Raafat Hammad Jadah

doi:10.12659/AJCR.951892

28 April 2026 : Case report Bahrain

A 4-Year-Old Bahraini Girl With Developmental Delay and Epilepsy of Infancy With Migrating Focal Seizures Associated With KCNT1 Gene Mutation

Rare disease

Noora Ebrahim AlHadi

^{ABCDEFG 1*}, Hessa Mohammed Albuainain^{ACDF 1}, Raafat Hammad Jadah^{ACDF 2}

DOI: 10.12659/AJCR.951892

Am J Case Rep 2026; 27:e951892

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Figure 1 Electroencephalogram (EEG) showing the background activity in the theta frequency range (5–6 Hz) of medium amplitude over the posterior head regions. Continuous epileptiform activity is noted from the P3 and T5 electrodes, as indicated by arrows.

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A 4-Year-Old Bahraini Girl With Developmental Delay and Epilepsy of Infancy With Migrating Focal Seizures Associated With KCNT1 Gene Mutation

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