Chondrocalcinosis related to familial hypomagnesemia with hypercalciuria and nephrocalcinosis.
J Pediatr Endocrinol Metab
; 28(5-6): 713-6, 2015 May.
Article
em En
| MEDLINE
| ID: mdl-25720051
ABSTRACT
Calcium pyrophosphate dehydrate (CPPD) crystal deposition disease (also known as chondrocalcinosis, CC) is a rare metabolic arthropathy mostly seen in elderly patients. Chondrocalcinosis may be associated with metabolic diseases such as hypomagnesemia when it occurs in young people. We report here a case with hypomagnesemia due to familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) who developed CC during clinical follow-up. To our best knowledge this is the first case of a young patient with CPPD associated with FHHNC.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Erros Inatos do Transporte Tubular Renal
/
Condrocalcinose
/
Hipercalciúria
/
Nefrocalcinose
Tipo de estudo:
Diagnostic_studies
Limite:
Adolescent
/
Humans
/
Male
Idioma:
En
Ano de publicação:
2015
Tipo de documento:
Article