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.

Nephrocalcinosis

Nephrocalcinosis is the deposition of calcium salts in renal parenchyma.


Total: 1

                       


(per page)
PMID (PMCID)
23087754
(3475018)
 OTHER
Hypercalciuria and nephrocalcinosis as early feature of Wilson disease onset: description of a pediatric case and literature review.
Di Stefano V, Lionetti E, Rotolo N, La Rosa M, Leonardi S.
Hepat Mon. 2012;12(8):e6233.
Hypercalciuria and nephrocalcinosis as early feature of Wilson disease onset: description of a pediatric case and literature review.