Malattia di Wilson

Rivista sfogliabile on line

2025/5

Wilson Wilson Wilson

Carciofi A, Pugliese F, D'alba I, Coccia P, Lionetti ME, Gatti S

2025/5 — pag. 120-121 — DOI

A 13-year-old boy was admitted with abdominal pain, vomiting and unexplained cytopoenia. Initial investigations showed splenomegaly, ileal wall thickening, hepatic structural alterations and persistent pancytopenia. Extensive infectious, haematologic...

Le tre regole di Wilson

A. Lora

2017/3

Insufficienza epatica acuta, un’evenienza rara... ma non troppo

C. Ripoli, A.P. Pinna, M. Furno, D. Congiu, S. Pusceddu, M.L. Fenu

2012/8 — pag. 515-517

Acute liver failure is a rare and complex disease that may present with a worsening course and needs a rational diagnostic and therapeutic intervention, in order to avoid most dangerous complications such as encephalopathy and metabolic changes, wh...

Malattia di Wilson: dieci motivi per (ri)parlarne ai pediatri

R. Iorio, G. Ranucci, D. Liccardo, M.G. Puoti, F. Di Dato

2012/8 — pag. 501-507

Wilson disease (WD) is an inherited autosomal recessive disorder of copper metabolism characterized by progressive copper accumulation in the liver and then in other organs, such as the nervous system, eyes and kidneys. In childhood, clinical prese...