Erratum to: Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?
نویسندگان
چکیده
Alethéa Guimarães Faria, Fernando Augusto Lima Marson, Carla Cristina de Souza Gomez, Maria Ângela Gonçalves de Oliveira Ribeiro, Lucas Brioschi Morais, Maria de Fátima Servidoni, Carmen Sílvia Bertuzzo, Eulália Sakano, Maura Goto, Ilma Aparecida Paschoal, Mônica Corso Pereira, Gabriel Hessel, Carlos Emílio Levy, Adyléia Aparecida Dalbo Contrera Toro, Andressa Oliveira Peixoto, Maria Cristina Ribeiro Simões, Elizete Aparecida Lomazi, Roberto José Negrão Nogueira, Antônio Fernando Ribeiro and José Dirceu Ribeiro
منابع مشابه
Quality of sweat test (ST) based on the proportion of sweat sodium (Na) and sweat chloride (Cl) as diagnostic parameter of cystic fibrosis: are we on the right way?
BACKGROUND To assess the quality of sweat test (ST) based on the proportion of sweat sodium and sweat chloride as diagnostic parameter of cystic fibrosis (CF). METHODS A retrospective study of 5,721 sweat samples and subsequent descriptive analysis were carried out. The test was considered "of good quality" (correct) when: (i) sweat chloride was lower than 60 mEq/L, and sweat sodium was highe...
متن کاملThirty Years of Sweat Chloride Testing at One Referral Center
Objective To conduct a descriptive analysis of the sweat test (ST), associating ST results with epidemiological data, CFTR (cystic fibrosis transmembrane conductance regulator) mutations and reasons to indicate the ST, as well as correlating sweat sodium and sweat chloride concentrations in subjects. Methods Retrospective survey and descriptive analysis of 5,721 ST at a university referral ce...
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The early description of cystic fibrosis (CF) dates back to late 30s. In 1936, Fanconi identified the association between the “congenital CF of the pancreas and broncheactasis" shortly followed by Andersen who in 1938 gave the complete anatomopathologic description of CF. In 1953, Di Sant'Agnese described an excess of sodium chloride in the sweat of children affected by CF. This discovery short...
متن کاملCystic Fibrosis and Cftr Gene
The early description of cystic fibrosis (CF) dates back to late 30s. In 1936, Fanconi identified the association between the “congenital CF of the pancreas and broncheactasis" shortly followed by Andersen who in 1938 gave the complete anatomopathologic description of CF. In 1953, Di Sant'Agnese described an excess of sodium chloride in the sweat of children affected by CF. This discovery short...
متن کاملCystic Fibrosis and Cftr Gene
The early description of cystic fibrosis (CF) dates back to late 30s. In 1936, Fanconi identified the association between the “congenital CF of the pancreas and broncheactasis" shortly followed by Andersen who in 1938 gave the complete anatomopathologic description of CF. In 1953, Di Sant'Agnese described an excess of sodium chloride in the sweat of children affected by CF. This discovery short...
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