Objectives This study aimed to evaluate the prevalence and incidence of WD and provide a
description of its main clinical and laboratory features. Methods A retrospective study was …

Objectives This study aimed to evaluate the prevalence and incidence of WD and provide a
description of its main clinical and laboratory features. Methods A retrospective study was …

Objective: To describe clinical symptoms, laboratory findings at diagnosis and treatment of
children and adolescents with Wilson's disease. Methods: This is a descriptive and …

BACKGROUND AND STUDY AIMS: Most paediatric patients with Wilson's disease (WD)
present with hepatic manifestations, but some may have neurologic or psychiatric features …

Background. Because molecular diagnosis is considered impractical and no patognomonic
features have been described, diagnosis of Wilson s disease (WD) using clinical and …

Background and aims. There are certain areas of uncertainty regarding the best therapeutic
approach in patients diagnosed with Wilson Disease (WD). Our aim was to assess treatment …

Abstract Background and Objectives Wilson's disease (WD) in children and adolescents is
predominantly asymptomatic or oligo‐symptomatic. The symptoms are nonspecific and …

OBJECTIVES: Clinical-laboratory and evolutionary analysis of twenty-eight patients with
Wilson's disease. METHODS: Twenty-eight children (twelve females and sixteen males) with …

Wilson's disease is the disease, the course and clinical picture of which varies from
asymptomatic forms to severe manifestations of dysfunction of many organs and systems …

Introduction Wilson disease is an autosomal recessive disease of liver copper metabolism
with predominant hepatic and neurological manifestations. Long-term data on the clinical …