DYT2 screening in early-onset isolated dystonia

Anna Rita Bentivoglio, Federica Zibordi, Miryam Carecchio, Chiara Reale, Federica Invernizzi, Valentina Monti, Simona Petrucci, Monia Ginevrino, Francesca Morgante, Giovanna Zorzi, Enza Maria Valente, Nardo Nardocci, Barbara Garavaglia

Risultato della ricerca: Contributo in rivistaArticolo in rivista

8 Citazioni (Scopus)

Abstract

BACKGROUND: Mutations in HPCA, a gene implicated in calcium signaling in the striatum, have been recently described in recessive dystonia cases previously grouped under the term "DYT2 dystonia". Positive patients reported so far show focal onset during childhood with subsequent generalization and a slowly progressive course to adulthood. METHODS: 73 patients with isolated dystonia of various distribution, manifesting within 21 years of age, were enrolled in this Italian study and underwent a mutational screening of HPCA gene by means of Sanger sequencing. RESULTS/CONCLUSIONS: Mean age at onset was 10.2 (±5.1) years and mean age at the time of genetic testing was 33 (±14.2) years. Mean disease duration at the time of enrollment was 22.7 (±12.8) years. None of the patients enrolled was found to carry HPCA mutations, rising suspicion that these probably represent a very rare cause of dystonia in childhood-adolescence. Larger studies will help determining the real mutational frequency of this gene also in different ethnic groups.
Lingua originaleEnglish
pagine (da-a)N/A-N/A
RivistaEuropean Journal of Paediatric Neurology
DOI
Stato di pubblicazionePubblicato - 2016

Keywords

  • DYT2
  • Dystonia
  • HPCA
  • Isolated
  • Pediatric
  • Recessive

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