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

BAYRAM, Ayse; GÜMÜŞ, HAKAN; ARSLAN, DURAN; OZCORA, Guldemet; KUMANDAŞ, SEFER; KARACABEY, Neslihan; CANPOLAT, MEHMET; PER, HÜSEYİN

doi:10.5152/turkpediatriars.2016.3080

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

Atıf İçin Kopyala

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)

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.