HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

[Early hypomagnesemia, hypercalciuria and nephrocalcinosis: two cases in a family].

AbstractBACKGROUND:
Hypomagnesemia-hypercalciuria and nephrocalcinosis is a rare inherited syndrome which is characterized by persistent hypomagnesemia despite supplementation, hypercalciuria, nephrocalcinosis and progressive renal failure.
OBSERVATIONS:
Case 1. A girl was referred at the age of 18 months because of polyuria, polydipsia and vitamin-resistant rickets. There was hypomagnesemia, hypercalciuria and mild renal insufficiency; ultrasonography showed nephrocalcinosis. For two years, she received hydrochlorothiazide and the course of the disease was marked by a significant reduction of urine output and hypercalciuria, recurrent urinary tract infections and a progression toward chronic renal failure. Case 2. The brother of this child was investigated at the age of nine months because of polyuria and polydipsia. He also had hypomagnesemia, hypercalciuria and nephrocalcinosis. Renal function was initially normal. After two years on continuous treatment with hydrochlorothiazide, hypercalciuria decreased without deterioration of renal function. No signs of rickets were noted and nephrocalcinosis remained stable.
CONCLUSION:
To our knowledge, these two patients are the youngest reported in the literature. The long-term deterioration of renal function is hazardous but rickets may be avoided by early administration of hydrochlorothiazide.
AuthorsC Mourani, E Khallouf, V Akkari, C Akatcherian, P Cochat
JournalArchives de pediatrie : organe officiel de la Societe francaise de pediatrie (Arch Pediatr) Vol. 6 Issue 7 Pg. 748-51 (Jul 1999) ISSN: 0929-693X [Print] France
Vernacular TitleHypomagnésémie, hypercalciurie et néphrocalcinose de révélation précoce: deux observations familiales.
PMID10429815 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Calcium
Topics
  • Calcinosis (diagnosis, diagnostic imaging, genetics)
  • Calcium (urine)
  • Consanguinity
  • Female
  • Humans
  • Infant
  • Kidney Diseases (diagnosis, diagnostic imaging, genetics)
  • Kidney Failure, Chronic (diagnosis)
  • Magnesium Deficiency (diagnosis, genetics)
  • Male
  • Nuclear Family
  • Radiography
  • Rickets (diagnostic imaging)
  • Syndrome
  • Ultrasonography

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: