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SM ISO690:2012 JIVALCOVSCHI, Ala, MACALEŢ, Tatiana, GURAGATA, Ana, TURCU, Oxana. Sindromul pseudobarter la sugarii cu fibroză chistică. In: Buletin de Perinatologie, 2013, nr. 2-3(58-59), pp. 202-204. ISSN 1810-5289. |
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Buletin de Perinatologie | ||||||
Numărul 2-3(58-59) / 2013 / ISSN 1810-5289 | ||||||
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Pag. 202-204 | ||||||
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Cystic fibrosis is the most common hereditary disease characterized by multiple organ failure and clinical polymorphism [3]. Children of the first months of life may develop Pseudo-Bartter's syndrome, which is a severe complication of cystic fibrosis, characterized by electrolyte disturbances such as hypokalemia, hyponatremia, and metabolic alkalosis [4]. Of 60 children with cystic fibrosis from Moldova, evaluated in the period 2007-2011, the disease started with Pseudo-Bartter's syndrome in 5.66% cases. Although Pseudo-Bartter's syndrome was described in infants with cystic fibrosis under 6 months of age, in our patient electrolyte disturbance recurrence were noted by the age of 12 months. Patient inability to compensate the electrolytes loss through sweat can be explained both by breastfeeding (the breast milk is known to be low in sodium chloride) and by recurrent episodes of respiratory infections |
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<meta name="citation_title" content="Sindromul pseudobarter la sugarii cu fibroză chistică"> <meta name="citation_author" content="Jivalcovschi Ala"> <meta name="citation_author" content="Macaleţ Tatiana"> <meta name="citation_author" content="Guragata Ana"> <meta name="citation_author" content="Turcu Oxana"> <meta name="citation_publication_date" content="2013/10/01"> <meta name="citation_journal_title" content="Buletin de Perinatologie"> <meta name="citation_volume" content="58-59"> <meta name="citation_issue" content="2-3"> <meta name="citation_firstpage" content="202"> <meta name="citation_lastpage" content="204"> <meta name="citation_pdf_url" content="https://ibn.idsi.md/sites/default/files/imag_file/Sindromul%20pseudobarter%20la%20sugarii%20cu%20fibroza%20chistica.pdf">