Neurological features and management of Wilson disease in children: an evaluation of 12 cases

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BAYRAM A. K. , GÜMÜŞ H. , ARSLAN D. , OZCORA G. K. , KUMANDAŞ S. , KARACABEY N., et al.

TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, cilt.51, ss.15-21, 2016 (ESCI İndekslerine Giren Dergi) identifier

  • Cilt numarası: 51 Konu: 1
  • Basım Tarihi: 2016
  • Doi Numarası: 10.5152/turkpediatriars.2016.3080
  • Dergi Adı: TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS
  • Sayfa Sayısı: ss.15-21

Özet

Aim: Wilson's disease is an autosomal recessive disorder of copper metabolism which leads to copper overload in different tissues of the body. The aim of this study was to present the neurologic features of Wilson's disease and to assess the clinical course of neurological findings in children receiving anti-copper treatment.