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Williams-Beuren Syndrome with Mirror Movements

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info:eu-repo/semantics/closedAccess

Date

2016-06

Author

Işıkay, Sedat
Sezer, Sadettin
Kırık, Serkan
Güngör, Olcay

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Citation

Işıkay, S., Sezer, S., Kırık, S., & Güngör, O. (2016). Williams-beuren syndrome with mirror movements. Indian Journal of Pediatrics, , 1-2. doi:10.1007/s12098-016-2182-3

Abstract

To the Editor: Williams-Beuren Syndrome (WBS) is a rare neurodevelopmental disorder caused by deletion of chromosome 7 at q11.23. It is characterized by distinctive facies, congenital cardiovascular malformations, intellectual disabilities, and various other manifestations [1, 2]. Here, we present a child with WBS who presented with abnormal involuntary hand movements...

Source

Indian Journal of Pediatrics

Issue

15 June 2016

URI

http://dx.doi.org/10.1007/s12098-016-2182-3
https://hdl.handle.net/20.500.11782/114

Collections

  • SBYO - FRB - Makale Koleksiyonu [4]
  • Scopus İndeksli Yayınlar Koleksiyonu [609]
  • WoS İndeksli Yayınlar Koleksiyonu [664]



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