From the Isfahan University of Medical Sciences. Isfahan. Iran
Abstract: (4293 Views)
In this paper we will present four cases of primary hyperoxaluria. All patients
had a significant past medical history of polyuria (with or without microscopic
hematuria) and polydypsia. All patients had a family history of their parents being
cousins. Initial evaluation of all patients by ultrasound and plain abdominal films
revealed nephrocalcinosis. Their clinical courses showed gradual loss of renal
function over the follow-up years. We will also review primary hyperoxalurias and
their management in this report.
Type of Study:
case report |
Subject:
Health