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dc.contributor.authorAmartino, Hernán.
dc.contributor.authorBay, Luisa.
dc.contributor.authorAntacle, Alejandra.
dc.contributor.authorEt al.
dc.date.accessioned2023-10-09T13:37:13Z
dc.date.available2023-10-09T13:37:13Z
dc.date.issued2021-04
dc.identifier.citationArch Argent Pediatr . 2021 Apr;119(2):e121-e128.es
dc.identifier.issn1668-3501
dc.identifier.urihttps://riu.austral.edu.ar/handle/123456789/2306
dc.descriptionDisponible en: https://www.sap.org.ar/docs/publicaciones/archivosarg/2021/v119n2a11e.pdfes
dc.description.abstractAbstract in English, Spanish Considering the advances made on mucopolysaccharidosis type I after the consensus study published by a group of experts in Argentina in 2008, recommendations about genetic testing, cardiological follow-up, airway care, hearing impairment detection, spinal and neurological conditions, as well as current treatments, were reviewed. Emphasis was placed on the need for early diagnosis and treatment, as well as an interdisciplinary follow-up. Keywords: classification; diagnosis; follow-up; mucopolysaccharidosis type I; treatment. Sociedad Argentina de Pediatría.es
dc.language.isoenes
dc.publisherSociedad argentina de pediatríaes
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMucopolysaccharidosis type Ies
dc.subjectClassificationes
dc.subjectDiagnosises
dc.titleNew recommendations for the care of patients with mucopolysaccharidosis type Ies
dc.typeArticlees


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional