alexa Suspected Wilson's Disease Presenting with Normal Serum
ISSN: 0974-8369

Biology and Medicine
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Case Report

Suspected Wilson's Disease Presenting with Normal Serum Ceruloplasmin Levels

Atul Singh Rajput*, Gunjan Singh Dalal and Jyoti Jain

Department of Biology and Medicine, Mahatma Gandhi Institute of Medical Sciences, India

*Corresponding Author:
Atul Singh Rajput
Department of Biology and Medicine
Mahatma Gandhi Institute of Medical Sciences
Wardha, Maharashtra, India
Tel: +918390617843
E-mail: [email protected]

Received Date: September 09, 2016; Accepted Date: November 02, 2016; Published Date: November 09, 2016

Citation: Rajput AS, Dalal GS, Jain J (2016) Suspected Wilson’s Disease Presenting with Normal Serum Ceruloplasmin Levels. Biol Med (Aligarh) 9: 362. doi: 10.4172/0974-8369.1000362

Copyright: © 2016 Rajput AS, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

 

Abstract

Wilson’s disease, also known as ‘Hepatolenticular degeneration’ is a disorder of copper handling. The clinical picture parallels the pathophysiology with symptoms of basal ganglia (10 to 100%), cerebellar dysfunction (18 to 73%) and liver dysfunction (18 to 84%). The patient profile usually describes a young male or female with signs of cerebellar dysfunction (Ataxia, Dysarthria and Nystagmus), basal ganglia dysfunction (Choreoathetosis), Kayser Fleisher (KF) rings in cornea and hepatic involvement (any form of acute or chronic liver disease). The basic pathophysiology relates to improper handling of copper by the liver owing to the dysfunctional ATP7B gene. The diagnostic tests include an increased urinary copper excretion (100 ug/dl), reduced serum ceruloplasmin levels (< 25 mg/dl) and increased hepatic copper concentration (> 200 ug/gm of liver tissue). Although reduced serum ceruloplasmin levels are observed in most patients of Wilson disease, some proportion of patients particularly with acute hepatitis type of presentation can spuriously have raised ceruloplasmin levels thus posing the clinicians a diagnostic challenge especially in rural resource limited set ups. Presentations like these can be quite misleading as clinical suspicion index remains pretty low despite extensive laboratory work up. We report a case of such a patient of acute hepatitis with normal serum ceruloplasmin levels but significantly elevated urinary copper excretion. The patient showed wonderful response to oral zinc replacement evidenced with clinicobiocemical improvement.

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