Showing papers in "Pediatria polska in 1974"
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TL;DR: It is supposed that a case presenting with co-existence of electrolytes disturbances on digestive and urinary tracts stands between congenital chloride diarrhoea and Bartter's syndrome, being an unknown kind of congenital hypokalemia.
Abstract: Long-term observation and laboratory investigations of a female infaut with chronic diarrhoea, hypokalemia, alkalosis and hypochloremia are presented. Diarrhoea with hypokalemie alkalosis persisted despite large-scale potassium chloride supplementation. An intravenous pyelogram showed duplication of the right pelvis and fetal lobate kidneys. She was normotensive. Plasma renin activity was increased. A permanent loss of electrolytes through urinary and digestive tracts was observed. Renal biopsy revealed the presence of fetal-like glomeruli, hyperplasia of juxtaglomerular apparatus and thickening of arterial walls. Hypertrophy and hyperplasia of the zona glomerulosa of adrenal cortex were present. It is supposed that a case presenting with co-existence of electrolytes disturbances on digestive and urinary tracts stands between congenital chloride diarrhoea and Bartter's syndrome, being an unknown kind of congenital hypokalemia.
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