作者: Tej K. Mattoo , Abdul M. Al-Sowailem , Mansoor S. Al-Harbi , Mustapha A. Mahmood , Yousef Katawee
DOI: 10.1007/BF00856821
关键词: Renal biopsy 、 Congenital nephrotic syndrome 、 Glomerulopathy 、 Surgery 、 Bilateral Nephrectomy 、 Nephrectomy 、 Focal segmental glomerulosclerosis 、 Nephrotic syndrome 、 Glomerulonephritis 、 Medicine
摘要: The study includes 17 infants with nephrotic syndrome. Their ages at the onset of disease ranged from 10 days to months (median 2 months), and included males 7 females. Ten patients had consanguineous parents 4 a history similar illness in sibling. Renal biopsy revealed diffuse mesangial proliferation patients, sclerosis 3, Finnish microcystic 2, focal segmental glomerulosclerosis atypical glomerulopathy 1 each. Unilateral nephrectomy was performed 8 intractable proteinuria associated multiple complications. Five are well after 4–36 follow-up, died septicaemia soon procedure, needed dialysis is stable 26 showed no reduction degree proteinuria. We conclude that unilateral better alternative bilateral some severe