Abstract:
:A 16-year-old female with acro-renal-ocular syndrome complicated by ventricular septal defect is described. Renal biopsy was performed for the first time in this syndrome, and the results suggested that proteinuria and renal dysfunction were caused by chronic pyelonephritis secondary to malrotation of the kidney and anomalous pelves. Chronic renal failure and hypoplasia of the optic papillae were also observed in the patient's mother, suggesting a participation of heredity in the pathogenesis of the syndrome.
journal_name
Nephronjournal_title
Nephronauthors
Naito T,Kida H,Yokoyama H,Abe T,Takeda S,Uno D,Hattori Ndoi
10.1159/000185264subject
Has Abstractpub_date
1989-01-01 00:00:00pages
115-8issue
1eissn
1660-8151issn
2235-3186journal_volume
51pub_type
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