Wilson disease

Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

Proteinuria

Increased levels of protein in the urine.


Total: 1

                       


(per page)
PMID (PMCID)
27437191
(4942312)
 OTHER
The Challenges of Diagnosing and Following Wilson Disease in the Presence of Proteinuria.
Khan S, Schilsky M, Silber G, Morgenstern B, Miloh T.
Pediatr Gastroenterol Hepatol Nutr. 2016;19(2):139-42.
The Challenges of Diagnosing and Following Wilson Disease in the Presence of Proteinuria.