Idiopathic Thrombocytopenia and Neurologic Manifestations in A Young Female Leading to the Diagnosis of Wilson’s disease

authors:

avatar Seyed Mohammad Salar Zaheryany 1 , avatar Reza Bidaki 2 , * , avatar Nahid Hemmatian Brujeni 1 , avatar Mohammad Rezvani 1 , avatar Mitra Hakim Shooshtari 1

Tehran University of Medical Sciences, Tehran, Iran
Rafsanjan University of Medical Sciences, Rafsanjan, Iran

How To Cite Zaheryany S M S, Bidaki R , Hemmatian Brujeni N, Rezvani M, Hakim Shooshtari M. Idiopathic Thrombocytopenia and Neurologic Manifestations in A Young Female Leading to the Diagnosis of Wilson’s disease. Iran J Psychiatry Behav Sci. 2012;6(2): 99-6. 

Abstract

We present a 19-year-old patient with hematologic and neurologic manifestations associated with Wilson’s disease. Idiopathic thrombocytopenia was diagnosed in October 2009. Bone marrow aspiration was normal. Gradually her neurologic and psychiatric symptoms emerged, dysarthria, writing apraxia, learning difficulties, emotionalism and eventually dystonia of hands. The serum ceruloplasmin was low, and the Kayser Fleischer's ring was positive. MRI of the brain showed abnormality in the bilateral basal ganglia, brain stem and superior cerebellar peduncles without post-contrast enhancement.
Declaration of interest: None
Citation: Zaheryany SMS, Bidaki R, Hemmatian Brujeni N, Rezvani M, Hakim Shooshtari M, Idiopathic thrombocytopenia and neurologic manifestations in a young female leading to the diagnosis of Wilson’s disease. Iran J Psychiatry Behav Sci 2012; 6(2): 96-99

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