ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases.

Fiorella Gurrieri, Michela Stagnaro, Livia Pisciotta, Marcella Gherzi, Maja Di Rocco, Elena Parrini, Giulia Prato, Edvige Veneselli, Elisa De Grandis

Risultato della ricerca: Contributo in rivistaArticolo in rivista

6 Citazioni (Scopus)

Abstract

Mutations in the ATP1A3 gene, which encodes the alpha3-subunit of sodium-potassium ATPase, are related to a spectrum of neurological diseases including Rapid onset Dystonia-Parkinsonism (RDP), Alternating Hemiplegia of Childhood (AHC) and Cerebellar ataxia, Areflexia, Pes cavus, Optic atrophy and Sensorineural hearing loss (CAPOS) syndrome. Moreover, an increasing number of patients with intermediate and non classical phenotypes have been reported. Herein we describe 7 patients with 6 different de novo ATP1A3 mutations, and we focus on paroxysmal and chronic movement disorders with the help of video documentation. Our cases confirm that ATP1A3-related neurological disorders make up a phenotypic continuum rather than overlapping syndromes, in which early onset dystonia, ataxia and paroxysmal episodes with triggering or worsening factors are key diagnostic clues. Moreover, our experience suggests that ATP1A3 gene analysis should be extended both to children with channelopathy-like spells and to patients with early onset, fever-related encephalopathy.
Lingua originaleEnglish
pagine (da-a)264-271
Numero di pagine8
RivistaEuropean Journal of Paediatric Neurology
Volume22
DOI
Stato di pubblicazionePubblicato - 2018

Keywords

  • ATP1A3
  • Alternating hemiplegia of childhood

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