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FAMILIYAL JUVENIL HIPERURISEMIK NEFROPATILI IKI KARDEŞ: OLGU SUNUMU

FAMILIAL JUVENILE HYPERURICAEMIC NEPHROPATHY IN TWO BROTHERS: CASE REPORT

Journal Name:

  • Türk Nefroloji, Diyaliz ve Transplantasyon Dergisi

Publication Year:

  • 2003

Key Words:

Keywords (Original Language):

Author NameUniversity of AuthorFaculty of Author
Abstract (2. Language): 
Familial juvenile hyperuricemia nephropathy (FJHN) is an autosomal dominant renal disease characterized by juvenile onset of hyperuricemia, gouty artritis, and progressive renal failure at an early age. Early treatment with allopurinol may prevents renal deterioration. Symptomless members of families in which the condition has been identified should be screened also, for renal function and urate handling. Here we report two brothers with FJHN which present after the development of renal failure.
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Abstract (Original Language): 
Familiyal jüvenil hiperürisemik nefropati (FJHN), jüvenil yaşta başlayan hiperürisemi, gut artriti ve erken yaşta ilerleyici böbrek yetersizliği ile belirgin otozomal dominant geçişli bir böbrek hastalığıdır. Erken dönemde allopürinol tedavisi ile hastalığın ilerlemesi önlenebilir. FJHN tanısı koyulan hastaların yakınları da hiperürisemi ve böbrek fonksiyonları açısından mutlaka tanınmalıdır. Biz bu makalede bize böbrek yetersizliği geliştikten sonra başvuran FJHN'li iki kardeş olguyu sunuyoruz.
FULL TEXT (PDF): 
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  • 4
233-235
  • Turkish

REFERENCES

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