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Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency

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References

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Authors and Affiliations

  1. Department of Pediatric Neurology, Cukurova University Medical Faculty, Toros mah., Barış Manço Bul. 78178 sok., Yeşilpark evleri, kat: 7, no: 13, Çukurova, Adana, Turkey

    Faruk Incecik & Ozlem M. Herguner

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  1. Faruk Incecik
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  2. Ozlem M. Herguner
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Correspondence to Faruk Incecik.

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

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The authors declared no potential conflict 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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Incecik, F., Herguner, O.M. Hydrocephalus as a rare clinical symptom in a child with multiple sulfatase deficiency. Acta Neurol Belg 117, 779–780 (2017). https://doi.org/10.1007/s13760-016-0736-9

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  • DOI: https://doi.org/10.1007/s13760-016-0736-9

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