Bartter syndrome (Q44713): Difference between revisions
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A síndrome de Bartter é uma doença tubular renal genética caracterizada pela associação de alcalose hipocalêmica, aumento dos níveis plasmáticos de renina e aldosterona, redução da pressão arterial e resistência vascular à angiotensina II. Duas formas da doença podem ser distinguidas de acordo com critérios clínicos: uma síndrome de Bartter pré-natal ou infantil (a maioria dos pacientes com genótipos I, II e IV), caracterizada por polidrâmnio, parto prematuro, poliúria, desidratação, hipercalciúria e nefrocalcinose; e a síndrome de Bartter clássica (a maioria pacientes com genótipo III, mas também alguns pacientes do tipo IV), manifestando-se como poliúria-polidipsia desde a primeira infância-infância até a idade adulta, desidratação e um atraso variável na curva de crescimento altura-peso. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Bartter syndrome is a genetic renal tubular disease characterised by the association of hypokalaemic alkalosis, increased levels of plasma renin and aldosterone, low blood pressure and vascular resistance to angiotensin II. Two forms of the disease can be distinguished according to clinical criteria: an antenatal or infantile Bartter syndrome (most patients with genotypes I, II and IV), characterised by polyhydramnios, premature delivery, polyuria, dehydration, hypercalciuria and nephrocalcinosis; and classical Bartter syndrome (mostly patients with genotype III, but also some type IV patients), manifesting as polyuria-polydipsia in infancy-childhood through to adulthood, dehydration and a variable delay in the height-weight growth curve. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/777233947 / rank | |||||||||||||||
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CID11:GB90.43 | |||||||||||||||
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dki-india-GB90.43 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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| Property / Linked ICD 10: N25 / rank | |||||||||||||||
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Latest revision as of 12:19, 13 August 2026
Bartter syndrome is a genetic renal tubular disease characterised by the association of hypokalaemic alkalosis, increased levels of plasma renin and aldosterone, low blood pressure and vascular resistance to angiotensin II. Two forms of the disease can be distinguished according to clinical criteria: an antenatal or infantile Bartter syndrome (most patients with genotypes I, II and IV), characterised by polyhydramnios, premature delivery, polyuria, dehydration, hypercalciuria and nephrocalcinosis; and classical Bartter syndrome (mostly patients with genotype III, but also some type IV patients), manifesting as polyuria-polydipsia in infancy-childhood through to adulthood, dehydration and a variable delay in the height-weight growth curve.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | GB90.43 |
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| English | Bartter syndrome |
Bartter syndrome is a genetic renal tubular disease characterised by the association of hypokalaemic alkalosis, increased levels of plasma renin and aldosterone, low blood pressure and vascular resistance to angiotensin II. Two forms of the disease can be distinguished according to clinical criteria: an antenatal or infantile Bartter syndrome (most patients with genotypes I, II and IV), characterised by polyhydramnios, premature delivery, polyuria, dehydration, hypercalciuria and nephrocalcinosis; and classical Bartter syndrome (mostly patients with genotype III, but also some type IV patients), manifesting as polyuria-polydipsia in infancy-childhood through to adulthood, dehydration and a variable delay in the height-weight growth curve. |
Statements
CID11:GB90.43
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dki-india-GB90.43
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Concluído
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13 August 2026
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