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Assessment of sleep disturbance in patients with Wilson’s disease
BackgroundWilson’s disease (WD) is frequently manifested with anxiety, depression and sleep disturbance; this investigation aimed to elucidate these...
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Clinical profile of adult and pediatric patients with hepatic Wilson’s disease
BackgroundThe clinical profile varies in patients with Wilson’s disease (WD). There is paucity of data regarding adult and pediatric patients with...
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A case of Wilson’s disease combined with intracranial lipoma and dysplasia of the corpus callosum with review of the literature
BackgroundWilson’s disease (WD) is an inherited disorder of copper metabolism. Agenesis of the corpus callosum is the complete or partial absence of...
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Membranous nephropathy caused by dimercaptosuccinic acid in a patient with Wilson’s disease: a case report and literature review
BackgroundDimercaptosuccinic acid (DMSA) therapy is a kind of chelation therapy for patients with Wilson ‘s disease (WD). While there have been...
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Correlation between neuroimaging, neurological phenotype, and functional outcomes in Wilson’s disease
IntroductionWilson’s disease (WD) is associated with a variety of movement disorders and progressive neurological dysfunction. The aim of this study...
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Rare co-occurrence of multiple sclerosis and Wilson’s disease – case report
BackgroundWilson’s disease is a hereditary disorder of copper metabolism resulting mainly in hepatic, neurological, and psychiatric symptoms....
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Early neurological deterioration in Wilson’s disease: a systematic literature review and meta-analysis
IntroductionNeurological deterioration, soon after anti-copper treatment initiation, is problematic in the management of Wilson’s disease (WD) and...
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Systemic lupus erythematosus combined with Wilson’s disease: a case report and literature review
BackgroundSystemic lupus erythematosus (SLE) and Wilson’s disease (WD) are both systemic diseases that can affect multiple organs in the body. The...
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Long-term outcome of patients with neurological form of Wilson’s disease compliant to the de-coppering treatment
BackgroundA substantial proportion of Wilson’s disease (WD) patients exhibit residual neurological symptoms. Data on the prognostic value of initial...
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Construction of a nomogram for predicting compensated cirrhosis with Wilson’s disease based on non-invasive indicators
BackgroundWilson’s disease (WD) often leads to liver fibrosis and cirrhosis, and early diagnosis of WD cirrhosis is essential. Currently, there are...
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Adherence to medical treatment for Wilson’s disease in children and adolescents: a cohort study from Turkey
BackgroundThis study aimed to assess medication adherence and demographic, clinical, and psychopathological parameters such as quality of life,...
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Large-scale networks changes in Wilson’s disease associated with neuropsychiatric impairments: a resting-state functional magnetic resonance imaging study
BackgroundIn Wilson’s disease (WD) patients, network connections across the brain are disrupted, affecting multidomain function. However, the details...
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Sleep disorders in Wilson’s disease: a questionnaire study
ObjectiveTo examine the clinical characteristics and influencing factors related to sleep disorders in patients with Wilson’s disease (WD), and...
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Brain magnetic resonance imaging and severity of neurological disease in Wilson’s disease — the neuroradiological correlations
IntroductionWilson’s disease (WD) is a genetic disorder with pathological copper accumulation and associated clinical symptoms in various organs,...
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Wilson’s disease clinic at the Assiut Liver Center in Egypt: a real well-established step on the way
Wilson’s disease (WD) is a rare genetic disorder of copper metabolism that results in dysfunction of copper excretion into bile leading to its...
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Neurological Type Wilson’s Disease: a Case Report
Wilson’s disease (WD) was defined in 1912 as a rare autosomal recessive disorder that leads to defective excretion of copper from the body. Normally,...
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Outcome of Wilson’s disease in Bangladeshi children: a tertiary center experience
BackgroundWilson disease (WD) is an inherited disorder of copper metabolism commonly involving the liver, cornea, and brain. Its incidence is...
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Assessment of the diagnostic value of serum ceruloplasmin for Wilson’s disease in children
BackgroundSerum ceruloplasmin is one of the major diagnostic parameters for Wilson’s disease (WD). Age and gender difference of serum ceruloplasmin...
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