%0 Journal Article
%T Involuntary movement in an emotionally labile girl : Think of WilsonĄ¯s Disease
%A Chowdhury Akram Uz Zaman
%A Chowdhury Rifat Niger
%A Raj Chowdhury
%A Rawshan Arra Khanam
%A Tamzeed Hossain
%J Bangladesh Critical Care Journal
%D 2018
%R https://doi.org/10.3329/bccj.v6i1.36615
%X WilsonĄ¯s Disease (WD) is a rare, autosomal recessive, inborn error of copper metabolism, which is caused by a mutation in the copper-transporting gene, ATP7B. The presentation is usually neurologic or hepatic or both, which is seen in 40% of the patients. The diagnosis depends primarily on the clinical features, the biochemical parameters and the presence of the Kayser ¨C Fleischer ring. Here, we are reporting a 13 years old girl who was affected by WilsonĄ¯s disease, with both neurological manifestations & hepatic involvement. Bangladesh Crit Care J March 2018; 6(1): 57-59
%K ATP7B
%K Dystonia
%K Kayser-Fleischer ring (K-F ring)
%K WilsonĄ¯s Disease (WD)
%U https://www.banglajol.info/index.php/BCCJ/article/view/36615