The Indian Journal of Pediatrics

, Volume 84, Issue 6, pp 473–474 | Cite as

Alternating Hemiplegia of Childhood with Novel Features

  • Hansashree Padmanabha
  • Jyotindra Nr. Goswami
  • Jitendra Kumar Sahu
  • Kathryn J. Swaboda
  • Pratibha Singhi
Scientific Letter

References

  1. 1.
    Heinzen EL, Swoboda KJ, Hitomi Y, et al. De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nat Genet. 2012;44:1030–4.CrossRefPubMedPubMedCentralGoogle Scholar
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    Panagiotakaki E, De Grandis E, Stagnaro M, et al. Clinical profile of patients with ATP1A3 mutations in alternating hemiplegia of childhood—a study of 155 patients. Orphanet J Rare Dis. 2015;10:123.CrossRefPubMedPubMedCentralGoogle Scholar
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    Viollet L, Glusman G, Murphy KJ, et al. Alternating hemiplegia of childhood: retrospective genetic study and genotype-phenotype correlations in 187 subjects from the US AHCF registry. PLoS One. 2015;10:e0127045.CrossRefPubMedPubMedCentralGoogle Scholar
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    Gurrieri F, Tiziano FD, Zampino G, Neri G. Recognizable facial features in patients with alternating hemiplegia of childhood. Am J Med Genet A. 2016;170:2698–705.Google Scholar

Copyright information

© Dr. K C Chaudhuri Foundation 2017

Authors and Affiliations

  • Hansashree Padmanabha
    • 1
  • Jyotindra Nr. Goswami
    • 1
  • Jitendra Kumar Sahu
    • 1
  • Kathryn J. Swaboda
    • 2
  • Pratibha Singhi
    • 1
  1. 1.Pediatric Neurology and Neurodevelopment Unit, Department of PediatricsPostgraduate Institute of Medical Education and ResearchChandigarhIndia
  2. 2.Department of Neurology, Center for Human Genetics ResearchMassachusetts General HospitalBostonUSA

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