Original article
Prenatal encephalopathies of unknown origin. Our 19 years experience. To what extent must genetic and biochemical studies be carried out?
Encefalopatías prenatales. Nuestra experiencia diagnóstica de 19 años. ¿Hasta dónde con los estudios bioquímicos y genéticos?
J. López Pisóna,b,c,
, M.C. García Jiménezb,d, M. Lafuente Hidalgoa,b, R. Pérez Delgadoa,b, L. Monge Galindoa,b, R. Cabrerizo de Diagoa,b, V. Rebage Moisésb,e, J.L. Peña Seguraa,b, A. Baldellou Vázquezb,d
Corresponding author
a Sección Neuropediatría, Hospital Universitario Miguel Servet, Zaragoza, Spain
b Grupo de Investigación Neurometabólico Pediátrico, Instituto Aragonés Ciencias de la Salud, Zaragoza, Spain
c Representante institucional del Gobierno de Aragón en la Estrategia de enfermedades raras del Ministerio de Sanidad y Política Socia, Madrid, Spain
d Sección Metabolismo, Hospital Universitario Miguel Servet, Zaragoza, Spain
e Sección Neonatal, Hospital Universitario Miguel Servet, Zaragoza, Spain
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