Catatonia responsive to corticosteroids in a patient with an SCN2A variant

Author:

Senko Kimberly123ORCID,Saddoris Kelsey L.123ORCID,Baus Ella123,Soe Katherine1234ORCID,Vaughn Samuel E.23ORCID

Affiliation:

1. Department of Pediatrics, Cincinnati Children's Hospital Medical Center University of Cincinnati College of Medicine Cincinnati Ohio USA

2. Division of Child & Adolescent Psychiatry, Cincinnati Children's Hospital Medical Center University of Cincinnati College of Medicine Cincinnati Ohio USA

3. Division of Psychiatry and Behavioral Neuroscience University of Cincinnati College of Medicine Cincinnati Ohio USA

4. Department of Pediatrics University of Cincinnati College of Medicine Cincinnati Ohio USA

Abstract

AbstractVariants in SCN2A are a known risk factor for developing autism spectrum disorder (ASD). Catatonia is a complex neuropsychiatric syndrome, which occurs at a higher rate in individuals with ASD. Catatonia has also been associated with COVID‐19 infection, though the majority of these cases are associated with increased serum inflammatory markers. We present a case of a 15‐year‐old female with ASD and corticosteroid responsive stuporous catatonia to explore the relationship between SCN2A variants, ASD, COVID‐19 exposure, and treatment refractory catatonia. Despite a lack of significantly elevated serum or CSF inflammatory markers, this patient showed significant improvement following initiation of corticosteroid therapy. This case presents a novel approach to the work‐up and treatment of catatonia in individuals with SCN2A variants independent of elevated inflammatory markers.

Publisher

Wiley

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