Tubular hypokalemia of genetic origin
Recent progress in molecular genetics have improved our understanding of the pathophysiology of several inherited diseases characterized by a renal hypokalemia. Some of these diseases result from inactivating mutations on the main cotransports involved in the reabsorption of sodium, namely the Gitelman and Bartter syndromes, that clinically mimics diuretic abuse with mild hypovolemia and low or normal blood pressure. Conversely some affections eventually lead to an increase in sodium reabsorption with hypervolemia and arterial hypertension: Liddle syndrome, apparent mineralocorticoid excess and dexamethasone suppressible hyperaldosteronism.
Medienart: |
Artikel |
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Erscheinungsjahr: |
1999 |
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Erschienen: |
1999 |
Enthalten in: |
Zur Gesamtaufnahme - volume:20 |
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Enthalten in: |
Nephrologie - 20(1999), 6 vom: 12., Seite 329-33 |
Sprache: |
Französisch |
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Weiterer Titel: |
Hypokaliémies tubulaires d'origine génétique |
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Beteiligte Personen: |
Kolb, I [VerfasserIn] |
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Themen: |
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Anmerkungen: |
Date Completed 21.12.1999 Date Revised 15.11.2006 published: Print Citation Status MEDLINE |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM105227765 |
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100 | 1 | |a Kolb, I |e verfasserin |4 aut | |
245 | 1 | 0 | |a Tubular hypokalemia of genetic origin |
246 | 3 | 3 | |a Hypokaliémies tubulaires d'origine génétique |
264 | 1 | |c 1999 | |
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500 | |a Date Completed 21.12.1999 | ||
500 | |a Date Revised 15.11.2006 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Recent progress in molecular genetics have improved our understanding of the pathophysiology of several inherited diseases characterized by a renal hypokalemia. Some of these diseases result from inactivating mutations on the main cotransports involved in the reabsorption of sodium, namely the Gitelman and Bartter syndromes, that clinically mimics diuretic abuse with mild hypovolemia and low or normal blood pressure. Conversely some affections eventually lead to an increase in sodium reabsorption with hypervolemia and arterial hypertension: Liddle syndrome, apparent mineralocorticoid excess and dexamethasone suppressible hyperaldosteronism | ||
650 | 4 | |a English Abstract | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Review | |
700 | 1 | |a Dimitrov, Y |e verfasserin |4 aut | |
700 | 1 | |a Caillard, S |e verfasserin |4 aut | |
700 | 1 | |a Hannedouche, T |e verfasserin |4 aut | |
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