Background: Therapeutic outcome of Wilson's disease (WD) significantly depends upon its
early recognition. However, because of its rarity in community and protean manifestations …

Background: Wilson's disease (WD) is a treatable autosomal recessive metabolic disorder
which could lead to protean hepatic or neurologic manifestations. WD could mimic many …

Wilson's disease (WD) is a relatively rare autosomal recessive inherited disorder causing
copper accumulation in different organs, mainly the liver and brain. Psychiatric disturbances …

The clinical manifestations of Wilson disease (WD) are varied and challenging. We
conducted the current study to present the phenotypic characteristics and follow-up for a …

Objective To evaluate the sensitivity of different MRI sequences in Wilson disease (WD) with
neurological manifestations and its correlation with clinical features and outcome. Methods …

Wilson disease–can present with such a variety of psychiatric and cognitive symptoms that it
has been named the “great masquerader.” Symptoms may include cognitive deficits …

Wilson disease (WD) is a rare disorder of copper metabolism that presents mainly with
hepatic and neuropsychiatric features. Copper accumulates not only in the liver and brain …

Introduction Study of MRI changes may be useful in diagnosis, prognosis and better
understanding of the pathophysiology of Wilson's disease (WD). We aimed to describe and …

INTRODUCTION: Recognition of psychiatric manifestations of Wilson's disease (WD) has
diagnostic and therapeutic implications. OBJECTIVE: To describe the clinical features and …

Objective To review the current evidence about psychiatric symptoms in Wilson's disease
(WD). Method We searched Ovid, PsychInfo, CINHAL and PubMed databases from May …