Naslov
Primary hyperoxaluria - Croatian experience

Autori
Batinić, Danica ; Milošević, Danko ; Leumann, Ernst ; Blau, Nenad ; Konjevoda, Paško ; Votava, Ana ; Barbarić, Vesna ; Nižić, Ljiljana ; Vrljičak, Kristina

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni

Izvornik
Fifth workshop on Primary hyperoxaluria : abstracts / Nephrology Dialysis Transplantation 14, 11 / - Zürich : Oxford University Press, 1999, 2789-2789

Skup
Fifth workshop on Primary hyperoxaluria

Mjesto i datum
Zürich, Švicarska, 12.03.1999. - 13.03.1999

Vrsta sudjelovanja
Predavanje

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
primary hyperoxaluria ; Croatia

Sažetak
Primary hyperoxaluria type 1 is a rare, inborn glyoxalate error of an autosomal recessive trait. We present 3 patients with this disease drom different families, who are consistent with inheritance. Laboratory data including urine oxalate excretion confirmed the diagnosis. Computer programe EQUIL2 was used to calculate urine calcium oxalate saturation. The treatment consisted of administration od piridoxine (300-600 mg/m2) with alkali citrate (0.15 g/kg). All of three patients had a reduced spontaneous passage of urinary stones, one of them without urolithiasis for the last of 2 years, after 4 years of follow-up, and with normal renal function. The patient with transplanted kidney without liver transplantation now shows clear ultrasound signs of nephrocalcinosis.

Izvorni jezik
Engleski

Znanstvena područja
Kliničke medicinske znanosti

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