Wilson's disease (WD) is characterised by a deleterious accumulation of copper in the liver
and brain. It is one of those rare genetic disorders that benefits from effective and lifelong …

Wilson's disease is an autosomal-recessive disorder of copper metabolism with hepatic,
neurological, psychiatric, ophthalmological, haematological, renal, and rheumatological …

Wilson's disease (WD), albeit relatively rare, is an important genetic metabolic disease
because of highly effective therapies that can be lifesaving. It is a great imitator and requires …

In Wilson disease (WD) defective AT7B function leads to biliary copper excretion and
pathologic copper accumulation, particularly in liver and brain, where it induces cellular …

Wilson's disease (WD) is an autosomal recessive disorder which is caused by poor
excretion of copper in mammalian cells. In this review, various issues such as effective …

Diffuse hepatic diseases have a variety of etiologies, with each showing characteristic
morphometric changes. These changes are closely related to micro-and macro-level …

Ultrasound is often the first imaging procedure performed in the evaluation of individuals
with suspected or known liver disease. Despite technical advances in ultrasound …

In children and adults, quantitative imaging examinations determine the effectiveness of
treatment for liver disease. However, pediatric liver disease differs in presentation from liver …

In brief, the classic form of Wilson's disease (WD) is an autosomal-recessive condition with
hepatic, neurologic, psychiatric and systemic manifestations. However, the diagnosis should …

Wilson disease (WD) is an autosomal genetic disorder characterized by excessive copper
deposition initially in liver (hepatic variant) followed by brain (neuropsychiatric variant) and …