Tirosinemia de tipo I, aciertos y errores

作者: Sandra Ardila , Olga Yaneth Echeverri , Johana Guevara , Eugenia Espinosa , Luis Alejandro Barrera

DOI: 10.1016/S0120-4912(15)30136-1

关键词:

摘要: RESUMEN La tirosinemia de tipo I es un error innato del metabolismo aminoacidos, ocasionada por la deficiencia o ausencia actividad enzimatica hidrolasa fumarilacetoacetato catabolismo tirosina; con cuadro clinico variable, se puede manifestar desde una forma neonatal grave hasta presentacion asintomatica tardia. El diagnostico rapido y el manejo nutricional son importantes para evolucion. Se presentan cuatro casos, dos confirmados como diagnosticos equivocados, resaltan los criterios terapeutico.

参考文章(9)
Cristine Trahms, Lisa Sniderman King, C Ronald Scott, Tyrosinemia Type I University of Washington, Seattle. ,(2014)
Ronen Arnon, Rachel Annunziato, Tamir Miloh, Melissa Wasserstein, Hiroshi Sogawa, Monique Wilson, Frederick Suchy, Nanda Kerkar, Liver transplantation for hereditary tyrosinemia type I: analysis of the UNOS database. Pediatric Transplantation. ,vol. 15, pp. 400- 405 ,(2011) , 10.1111/J.1399-3046.2011.01497.X
Maria Luz Couce, Jaime Dalmau, Mireia del Toro, Guillem Pintos-Morell, Luís Aldámiz-Echevarría, , Tyrosinemia type 1 in Spain: Mutational analysis, treatment and long-term outcome Pediatrics International. ,vol. 53, pp. 985- 989 ,(2011) , 10.1111/J.1442-200X.2011.03427.X
Hanaa El-Karaksy, Mohmmad Rashed, Rokaya El-Sayed, Mona El-Raziky, Nehal El-Koofy, Manal El-Hawary, Osama Al-Dirbashi, Clinical practice. NTBC therapy for tyrosinemia type 1: how much is enough? European Journal of Pediatrics. ,vol. 169, pp. 689- 693 ,(2010) , 10.1007/S00431-009-1090-1
Denis Devictor, Pierre Tissieres, Mickael Afanetti, Dominique Debray, Acute liver failure in children. Clinics and Research in Hepatology and Gastroenterology. ,vol. 35, pp. 430- 437 ,(2011) , 10.1016/J.CLINRE.2011.03.005
ML Couce, L Aldamiz-Echevarria, A Baldellou, J Blasco, MA Bueno, J Dalmau, A De La Vega, M Del Toro, C Diaz, R Lama, E Leao, M Marrero, VM Navas, G Pintos, None, Recomendaciones y manejo de la tirosinemia hereditaria Tipo I o Tirosinemia hepatorrenal Anales De Pediatria. ,vol. 73, pp. 279- 279 ,(2010) , 10.1016/J.ANPEDI.2010.03.005
Fatiha Bendadi, Tom J. de Koning, Gepke Visser, Hubertus C.M.T. Prinsen, Monique G.M. de Sain, Nanda Verhoeven-Duif, Gerben Sinnema, Francjan J. van Spronsen, Peter M. van Hasselt, Impaired Cognitive Functioning in Patients with Tyrosinemia Type I Receiving Nitisinone The Journal of Pediatrics. ,vol. 164, pp. 398- 401 ,(2014) , 10.1016/J.JPEDS.2013.10.001
A. Masurel-Paulet, J. Poggi-Bach, M.-O. Rolland, O. Bernard, N. Guffon, D. Dobbelaere, J. Sarles, H. Ogier de Baulny, G. Touati, NTBC treatment in tyrosinaemia type I: long-term outcome in French patients. Journal of Inherited Metabolic Disease. ,vol. 31, pp. 81- 87 ,(2008) , 10.1007/S10545-008-0793-1
Corinne de Laet, Carlo Dionisi-Vici, James V Leonard, Patrick McKiernan, Grant Mitchell, Lidia Monti, Hélène Ogier de Baulny, Guillem Pintos-Morell, Ute Spiekerkötter, Recommendations for the management of tyrosinaemia type 1 Orphanet Journal of Rare Diseases. ,vol. 8, pp. 8- 8 ,(2013) , 10.1186/1750-1172-8-8