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[Recommendations and management of type I hereditary or hepatorenal tyrosinemia]. / Recomendaciones y manejo de la tirosinemia hereditaria Tipo I o Tirosinemia hepatorrenal.
Couce, M L; Aldámiz-Echevarría, L; Baldellou, A; Blasco, J; Bueno, M A; Dalmau, J; De La Vega, A; Del Toro, M; Díaz, C; Lama, R; Leao, E; Marrero, M; Navas, V M; Pintos, G.
Affiliation
  • Couce ML; Departamento de Pediatría, Hospital Clínico Universitario de Santiago, Santiago de Compostela, España. maria.luz.couce.pico@sergas.es
An Pediatr (Barc) ; 73(5): 279.e1-4, 2010 Nov.
Article de Es | MEDLINE | ID: mdl-20813594
ABSTRACT
Tyrosinemia type I is a potentially lethal disease if not diagnosed and treated properly. Diagnostic and therapeutic advances in recent years have significantly improved the prognosis for these patients. It is therefore important that the pediatrician has a clinical practice guideline with recommendations for diagnosis and treatment of this disease that leads to the appropriate intervention.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Diagnostic_studies / Guideline / Prognostic_studies Limites: Child / Humans Langue: Es Journal: An Pediatr (Barc) Sujet du journal: PEDIATRIA Année: 2010 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Diagnostic_studies / Guideline / Prognostic_studies Limites: Child / Humans Langue: Es Journal: An Pediatr (Barc) Sujet du journal: PEDIATRIA Année: 2010 Type de document: Article
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