Case Report: Benign Infantile Seizures Temporally Associated With COVID-19

Marcos García-Howard1, Mercedes Herranz-Aguirre2, Laura Moreno-Galarraga3,4

  • 1Department of Pediatrics, CHN, Navarra Health Service Hospital, Pamplona, Spain.

Frontiers in Pediatrics
|August 28, 2020
PubMed

Insights

COVID-19 can cause non-febrile seizures in infants with a genetic predisposition, even without respiratory symptoms. Early genetic testing and tailored treatment are crucial for managing these neurological complications.

Area of Science:

  • Neurology
  • Infectious Diseases
  • Genetics

Background:

  • Non-febrile seizures in children are associated with minor infections and genetic factors.
  • COVID-19 commonly presents with fever, cough, or GI issues in children, sometimes with a hyperimmune response.
  • Neurological complications in pediatric COVID-19 cases remain under-documented.

Observation:

  • A 3-month-old infant with COVID-19 developed repeated non-febrile seizures.
  • Investigations ruled out meningo-encephalitis or epilepsy; SARS-CoV-2 PCR was positive.
  • Elevated ferritin and D-dimer levels were noted, alongside a pathogenic PRRT2 gene mutation in infant and mother.

Findings:

  • COVID-19 can manifest as afebrile seizures in infants, particularly those with genetic predispositions.
  • A PRRT2 gene mutation was identified in an infant with COVID-19-associated seizures.
  • Infants can exhibit hyperimmune responses to SARS-CoV-2, similar to adults, even without severe respiratory symptoms.

Implications:

  • This case highlights COVID-19 as a potential trigger for early-onset seizures in genetically susceptible infants.
  • Precision medicine approaches, including whole exome sequencing, are vital for understanding host responses to COVID-19.
  • Early diagnosis and genetic insights can guide management strategies for pediatric neurological complications of COVID-19.