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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.
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.
Abstract:
Background: Non-febrile illness seizures may present in previously healthy children as afebrile seizures associated with minor infections, such as mild gastroenteritis or respiratory tract infections, and are linked to a genetic predisposition. For the novel human coronavirus SARS-CoV-2, causing COVID-19, fever, cough, and gastrointestinal complaints are the most common symptoms in children, and a hyperimmune response may be present. No detailed temporally associated neurological complications have been documented in pediatric case series so far. Case description: We present the case of a 3-months-old girl with non-febrile repeated seizures in a COVID-19 family setting. The infant started with a mild fever and cough that lasted for 2 days. At day 6 from onset, the girl presented with two focal motor seizures with impaired consciousness and awareness. All investigations ruled out signs of meningo-encephalitis or active epilepsy, including normal electroencephalogram and cerebral magnetic resonance imaging. PCR from nasal and throat swabs was positive for SARS-CoV-2. Remarkably, blood ferritin and D-dimer levels were increased. At day 9, the infant presented another afebrile motor seizure, and levetiracetam dose was modified there was a favorable response within 3 months of the follow-up. Much interest has been raised with regards to host genetic determinants to disease severity and susceptibility to COVID-19. We thus performed whole exome sequencing, revealing a pathogenic frameshift mutation in the PRRT2 gene in both the mother and the infant. The mother had presented two late infantile febrile convulsions with normal outcome afterwards. Discussion: The hyperimmune response described in adult cases with COVID-19 can be seen in infants, even in the absence of respiratory symptoms. Moreover, COVID-19 may present in infants as non-febrile seizures, triggering early onset seizures in infants with a genetic predisposition. In this pandemic situation, precision medicine using massive sequencing can shed light on underlying molecular mechanisms driving the host response to COVID-19.
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