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September 23, 2026Archives de PédiatrieOpen Access

Acute neuro-inflammatory presentation of ATP1A3 variants: Case reports of three patients with different phenotypes

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Authors

CGCapucine GlassonMGMarc GibaudMAMarie Alesandrini

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Cite This Study

Glasson et al. (2026) studied this question.

synapsesocial.com/papers/6ab39db54f6cc12e38b51365https://doi.org/10.1016/j.arcped.2026.105616
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up2022 · 6 citations
  2. 2Relapsing encephalopathy with cerebellar ataxia related to an <i><scp>ATP</scp>1A3</i> mutation2015 · 97 citations
  3. 3ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum2021 · 67 citations
  4. 4Variants of <i>ATP1A3</i> in residue 756 cause a separate phenotype of relapsing encephalopathy with cerebellar ataxia (RECA)—Report of two cases and literature review2021 · 14 citations