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FAMILIAL HIPOMAGNEZEMIK HıPERKALSıÜRıYE BAĞLı KRONIK BÖBREK YETERSIZLIĞI (VAKA TAKDIMI)

CHRONIC RENAL FAILURE DUE TO FAMILIAL HYPOMAGNESEMIC HYPERCALCIURIA (A CASE REPORT)

Journal Name:

  • Türk Nefroloji, Diyaliz ve Transplantasyon Dergisi

Publication Year:

  • 1999

Key Words:

Keywords (Original Language):

Author NameUniversity of AuthorFaculty of Author
Abstract (2. Language): 
Familial Hypomagnesemia- hypercalciuria is a hereditary disease of unknown etiology characterized by persistant Hypomagnesemia, incomplete distal tubuler acidosis, hypercalciuria and nephrocalcinosis. We have reported and discussed a case with familal hypomagnesemic hypercalciuria leading to nephrocalcinosis and chronic renal failure
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Abstract (Original Language): 
Familial hipomagnezemik hiperkalsiüri; hipomagnezemi, inkomplet distal tubuler asidoz ve hiperkalsiüri ile karakterize bir tablodur. Hastalık otozomal resesif geçiş gösterir ve erken yaşlarda nefrokalsinozis e bağlı böbrek yetersizliğine yol açar. Bu makalede familial hipomagnezemik hiperkalsiüriye bağlı nefrokalsinozis sonucu kronik böbrek yetersizliği gelişen bir hasta literatür eşliğinde tartışılmıştır.
FULL TEXT (PDF): 
PDF icon pdf_tndt_274.pdf
  • 4
219-220
  • Turkish

REFERENCES

References: 

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