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[Cystic fibrosis primarily presenting with pseudo-Bartter syndrome: a report of three cases and literature review]. [PDF]
Zhang JY +6 more
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Bartter's Syndrome and Pseudo-Bartter's Syndrome
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Annual Review of Medicine, 1980
Correspondence pertaining to material published in theJournalwill be published, if found suitable, as space permits. Submit double-spaced copy clearly marked "For publication" and signed by all authors; references should conform toJournalformat; maximum length: 500 words. Copyright assignment signed by all authors is required.
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Correspondence pertaining to material published in theJournalwill be published, if found suitable, as space permits. Submit double-spaced copy clearly marked "For publication" and signed by all authors; references should conform toJournalformat; maximum length: 500 words. Copyright assignment signed by all authors is required.
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Hypokalaemia: Bartter's Syndrome or Pseudo-Bartter's Syndrome?
Journal of the Royal Society of Medicine, 1984The difficulties in the diagnosis of hypokalaemia are often considerable. This paper reports three patients who presented with hypokalaemia. Investigations are described which may help to distinguish Bartter's syndrome from pseudo-Bartter's syndrome.
J D, Robb +3 more
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Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego, 2004
Bartter syndrome is an uncommon tubular disorder inherited as an autosomal recessive entity. It is associated with hypokalemic metabolic alkalosis with high renin and aldosterone plasma concentration with low or normal blood pressure. Recent studies have demonstrated genetic heterogeneity in Bartter syndrome.
I. Lenga, K.S. Kamel
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Bartter syndrome is an uncommon tubular disorder inherited as an autosomal recessive entity. It is associated with hypokalemic metabolic alkalosis with high renin and aldosterone plasma concentration with low or normal blood pressure. Recent studies have demonstrated genetic heterogeneity in Bartter syndrome.
I. Lenga, K.S. Kamel
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Archives of Internal Medicine, 1982
Two sisters were found to have Bartter's syndrome. Both had hypokalemia, hyperreninemia, normal BPs, and decreased pressor responses to angiotensin II. During a water diuresis, patient 1 had an abnormally low distal tubular fractional reabsorption of chloride initially, but this normalized after hypokalemia was corrected for one year.
T, Ogihara +5 more
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Two sisters were found to have Bartter's syndrome. Both had hypokalemia, hyperreninemia, normal BPs, and decreased pressor responses to angiotensin II. During a water diuresis, patient 1 had an abnormally low distal tubular fractional reabsorption of chloride initially, but this normalized after hypokalemia was corrected for one year.
T, Ogihara +5 more
openaire +2 more sources

