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dc.contributor.author Zúñiga Lara, Elsa Mariana
dc.contributor.author Martínez Camacho, Karla Ariadna
dc.contributor.author SANCHEZ SALINAS, EDUARDO
dc.contributor.author Rodríguez Ramírez, Rosana Teresa
dc.contributor.author Mendieta Zerón, Hugo
dc.creator Zúñiga Lara, Elsa Mariana;#0000-0002-2648-5734
dc.creator Martínez Camacho, Karla Ariadna;#0000-0002-0913-537X
dc.creator SANCHEZ SALINAS, EDUARDO; 895454
dc.creator Rodríguez Ramírez, Rosana Teresa;x1360738
dc.creator Mendieta Zerón, Hugo; 45175
dc.date.accessioned 2023-01-10T03:07:51Z
dc.date.available 2023-01-10T03:07:51Z
dc.date.issued 2022-12-28
dc.identifier.issn 2437-0665
dc.identifier.uri http://hdl.handle.net/20.500.11799/137470
dc.description.abstract Objective. Congenital diseases are hereditary disorders whose timely detection is vital for early treatment, thus avoiding serious consequences in the future. Material and methods. A retrospective study was made of suspected cases of congenital diseases detected through the neonatal screening in a third level hospital of Toluca, Mexico, from the tear 2019 to 2020. Results. 30 suspected cases were found between the years 2019-2020, out of a total of 4384 cases, 18 of which were in 2019 and 12 in 2020. Concerning the data collected, the disease with the most prevalence was cystic fibrosis occurring in 14 cases out of 30. Conclusions. The most common congenital metabolic disease in our hospital is cystic fibrosis. This study justifies the need to enhance the neonatal diagnosis of metabolic disorders and the need to take the next step with genetic studies to better characterize the affected population. es
dc.language.iso eng es
dc.publisher Association de la Recherche Pharmaceutique & d'Enrichissement des Connaissances es
dc.rights openAccess es
dc.rights.uri http://creativecommons.org/licenses/by/4.0
dc.subject Neonatal screening es
dc.subject Congenital hypothyroidism es
dc.subject Phenylketonuria es
dc.subject Congenital adrenal hyperplasia es
dc.subject Cystic fibrosis es
dc.subject.classification MEDICINA Y CIENCIAS DE LA SALUD
dc.title Neonatal screening. A two-year retrospective study es
dc.type Artículo es
dc.provenance Científica es
dc.road Dorada es
dc.organismo Medicina es
dc.ambito Estatal es
dc.audience students es
dc.audience researchers es
dc.type.conacyt article
dc.identificator 3
dc.relation.vol 9
dc.relation.no 2


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  • Título
  • Neonatal screening. A two-year retrospective study
  • Autor
  • Zúñiga Lara, Elsa Mariana
  • Martínez Camacho, Karla Ariadna
  • SANCHEZ SALINAS, EDUARDO
  • Rodríguez Ramírez, Rosana Teresa
  • Mendieta Zerón, Hugo
  • Fecha de publicación
  • 2022-12-28
  • Editor
  • Association de la Recherche Pharmaceutique & d'Enrichissement des Connaissances
  • Tipo de documento
  • Artículo
  • Palabras clave
  • Neonatal screening
  • Congenital hypothyroidism
  • Phenylketonuria
  • Congenital adrenal hyperplasia
  • Cystic fibrosis
  • Los documentos depositados en el Repositorio Institucional de la Universidad Autónoma del Estado de México se encuentran a disposición en Acceso Abierto bajo la licencia Creative Commons: Atribución-NoComercial-SinDerivar 4.0 Internacional (CC BY-NC-ND 4.0)

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