Chondrocalcinosis related to familial hypomagnesemia with hypercalciuria and nephrocalcinosis

J Pediatr Endocrinol Metab. 2015 May;28(5-6):713-6. doi: 10.1515/jpem-2013-0254.

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.

MeSH terms

  • Adolescent
  • Chondrocalcinosis / complications*
  • Chondrocalcinosis / diagnostic imaging
  • Humans
  • Hypercalciuria / complications*
  • Hypercalciuria / diagnostic imaging
  • Male
  • Nephrocalcinosis / complications*
  • Nephrocalcinosis / diagnostic imaging
  • Radiography
  • Renal Tubular Transport, Inborn Errors / complications*
  • Renal Tubular Transport, Inborn Errors / diagnostic imaging

Supplementary concepts

  • Hypomagnesemia primary