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Sinus pericranii and myoclonic epilepsy: novel features of 3q29 microdeletion syndrome

Acta Neurologica Belgica volume 116, pages 363–364 (2016)Cite this article

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Fig. 1

Reference

  1. Cox DM, Butler MG (2015) A clinical case report and literature review of the 3q29 microdeletion syndrome. Clin Dysmorphol 24(3):89–94

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Affiliations

  1. Division of Child Neurology, University of Arkansas for Medical Sciences, Little Rock, AR, USA

    Debopam Samanta

  2. Children’s Way, Little Rock, AR, 72202, USA

    Debopam Samanta

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  1. Debopam Samanta
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Correspondence to Debopam Samanta.

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The author declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

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The author received no financial support for the research, authorship, and/or publication of this article.

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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

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Informed consent was obtained from the parents of child included in the study

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Samanta, D. Sinus pericranii and myoclonic epilepsy: novel features of 3q29 microdeletion syndrome. Acta Neurol Belg 116, 363–364 (2016). https://doi.org/10.1007/s13760-015-0554-5

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  • DOI: https://doi.org/10.1007/s13760-015-0554-5

Keywords

  • Myoclonic Epilepsy
  • Myoclonic Jerk
  • Epilepsy Syndrome
  • Pectus Excavatum
  • Anterior Fontanel