ARTÍCULO ESPECIAL
Recomendaciones y manejo de la tirosinemia hereditaria Tipo I o Tirosinemia hepatorrenal
Recommendations and management of Type I hereditary or hepatorenal Tyrosinemia
M.L. Coucea,
, L. Aldámiz-Echevarríab, A. Baldellouc, J. Blascod, M.A. Buenoe, J. Dalmauf, A. De La Vegag, M. Del Toroh, C. Díazg, R. Lamag, E. Leaoi, M. Marreroj, V.M. Navasd, G. Pintosk
a Unidad de Trastornos Metabólicos, Departamento de Pediatría, Hospital Clínico Universitario de Santiago, Santiago de Compostela, España
b Unidad de Metabolismo, Hospital de Cruces, Barakaldo, España
c Departamento de Pediatría, Universidad de Zaragoza, Zaragoza, España
d Servicio de Pediatría. Hospital Materno Infantil Carlos Haya, Málaga, España
e Unidad de Metabolopatías, Servicio de Pediatría. Hospital Universitario Virgen del Rocío, Sevilla, España
f Unidad de Nutrición y Metabolopatías, Hospital Infantil La Fe, Valencia, España
g Servicio de Hepatología y Trasplante hepático Infantil, Hospital Universitario La Paz, Madrid
h Unidad de Neurología Infantil, Servicio de Pediatría, Hospital Vall d'Hebrón, Barcelona, España
i Unidad de Enfermedades Metabólicas, Servicio de Pediatría, Hospital de S. Joao, Porto, Portugal
j Servicio de Pediatría, Hospital Ntra Señora de Sonsoles, Ávila, España
k Unidad de Nefrología y Metabolismo, Hospital Universitari Germans Trias i Pujol, Badalona, España
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