CC BY 4.0 · Arq Neuropsiquiatr 2024; 82(S 02): S53-S176
DOI: 10.1055/s-0045-1807028
ID: 626
Area: Epilepsies
Presentation method: Eletronic Poster

Epilepsy of migrating focal seizures and ketogenic diet: a hopeful association

Janaina Moraes Araujo
1   Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto SP, Brazil.
,
Lilian Aparecida Sansao
1   Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto SP, Brazil.
,
Emanuelle Bianchi da Silva Rocha
1   Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto SP, Brazil.
,
Debora de Cassia Tomaz Fernandes
1   Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto SP, Brazil.
,
Renan Campi Gomes
1   Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto SP, Brazil.
,
Felipe Pires Albuquerque
1   Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto SP, Brazil.
,
Livia Pires Albuquerque
1   Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto SP, Brazil.
› Institutsangaben
 

    *Correspondence: janaina_ni@hotmail.com.

    Abstract

    Case Presentation: A healthy male infant, at one month old, started episodes described as ocular eversion and migrating focal involuntary movements, which occurs in cluster without complete recovery of the consciousness between the attacks and with many events per day. Parents denied complications during pregnancy and childbirth, as well as similar cases in the family. Magnetic resonance imaging of the brain and screening for inborn error of metabolism were normal. All several electroencephalogram performed demonstrated assymetrical and severely disorganization of the base activity and abundant, multifocal and independent epileptiform discharges with predominance at frontal, temporal and occipital regions. The genetic panel for epilepsy evidenced one pathogenic variant in heterozygous in the KCNT1 gene. For treatment, we tried many antiepileptic drugs (valproate, clobazam and phenobarbital), without adequate response and in December of 2022 and January of 2023, he evolved to status epilepticus. After genetic tests evidenced alteration in the coding of potassium channels, we performed a therapeutic test with quinidine 5 mg/kg/day associated with ketogenic diet, with satisfactory response. However, due to significant weight loss, it was necessary to suspend the diet, and then crises returned. In March of 2023, we restarted ketogenic diet in the form of industrialized supplement associated with quinidine, valproate, clobazam and phenobarbital with resolution of the crises.

    Discussion: Epilepsy of migrating focal seizures is a rare epileptic encephalopathy (so far, there is only 200 cases described on the literature), caused by a pathogenic variant in the KCNT1 gene. This disorder is characterized by seizures with poor response to various antiepileptic drugs and neurodevelopmental impairment. In our case, we tried many drugs and even quinidine had a poor control of the crises. The adequate control was obtained only with the association of ketogenic diet.

    Final Comments: The ketogenic diet is an important option in patients with refractory epilepsy and impossibility to undergo surgery, with reduction or control of the seizures up to one-third of the patients. Epilepsy with migrating focal seizures can cause severe developmental delay and with this case report, we aim to share this treatment option.


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    Artikel online veröffentlicht:
    12. Mai 2025

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