NDLI: Tirosinemia de tipo I, aciertos y errores

Content Provider	Semantic Scholar
Author	Ardila, Sandra Echeverri, Olga Yanet Guevara, Johana M. Espinosa, Eugenia Colomer Barrera, Luis Alejandro Gómez
Copyright Year	2014
Abstract	RESUMEN La tirosinemia de tipo I es un error innato del metabolismo de aminoacidos, ocasionada por la deficiencia o ausencia de la actividad enzimatica de la hidrolasa del fumarilacetoacetato del catabolismo de tirosina; con un cuadro clinico variable, se puede manifestar desde una forma neonatal grave hasta una presentacion asintomatica tardia. El diagnostico rapido y el manejo nutricional son importantes para la evolucion. Se presentan cuatro casos, dos confirmados como tirosinemia I y dos con diagnosticos equivocados, y se resaltan los criterios diagnosticos y el manejo terapeutico.
Starting Page	55
Ending Page	59
Page Count	5
File Format	PDF HTM / HTML
DOI	10.1016/S0120-4912(15)30136-1
Alternate Webpage(s)	http://appswl.elsevier.es/publicaciones/item/pdf?estadoItem=S350&idApp=UINPBA00004N&idiomaItem=es&origen=zonadelectura&pii=S0120491215301361&textMensaje=Documento+descargado+de+http://www.elsevier.es+el+25-09-2017&urlApp=http://www.elsevier.es&web=zonadelectura
Alternate Webpage(s)	http://appswl.elsevier.es/publicaciones/item/pdf?estadoItem=S350&idApp=UINPBA00004N&idiomaItem=es&origen=zonadelectura&pii=S0120491215301361&textMensaje=Documento+descargado+de+http://www.elsevier.es+el+07-08-2017&urlApp=http://www.elsevier.es&web=zonadelectura
Alternate Webpage(s)	https://www.elsevier.es/index.php?p=revista&pRevista=pdf-simple&pii=S0120491215301361
Alternate Webpage(s)	https://doi.org/10.1016/S0120-4912%2815%2930136-1
Volume Number	47
Language	English
Access Restriction	Open
Content Type	Text
Resource Type	Article

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