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The neurological aspects related to POGZ mutation: case report and review of CNS malformations and epilepsy

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References

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Funding

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

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Authors and Affiliations

  1. Child Neurology Division, Department of Pediatrics, University of Arkansas for Medical Sciences, 1 Children’s Way, Little Rock, AR, 72202, USA

    Debopam Samanta

  2. Division of Neuroradiology and Pediatric Radiology, University of Arkansas for Medical Sciences, Little Rock, AR, USA

    Raghu Ramakrishnaiah

  3. Division of Genetics, Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA

    Bradley Schaefer

Authors
  1. Debopam Samanta
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  2. Raghu Ramakrishnaiah
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  3. Bradley Schaefer
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Contributions

DS: drafted the manuscript, RR: interpretation of neuroimaging and revision of the manuscript, BS: revision of manuscript

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Correspondence to Debopam Samanta.

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The authors declared no potential conflicts of interest with respect to 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 the child included in the study.

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Samanta, D., Ramakrishnaiah, R. & Schaefer, B. The neurological aspects related to POGZ mutation: case report and review of CNS malformations and epilepsy. Acta Neurol Belg 120, 447–450 (2020). https://doi.org/10.1007/s13760-019-01122-6

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  • DOI: https://doi.org/10.1007/s13760-019-01122-6

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