El laboratorio en el diagnóstico de las enfermedades raras

Autores/as

  • R Artuch Departamento de Bioquímica Clínica, Hospital San Joan de Déu
  • J Moreno
  • R.M Puig
  • M Quintana
  • R Montero
  • A Ormazábal
  • M.A Vilaseca

Palabras clave:

Enfermedades raras, Errores congénitos del metabolismo, Análisis de metabolitos, Estudios genéticos, Pruebas funcionales

Resumen

Inborn errors of metabolism (IEM) are a group of diseases whose diagnosis is usually performed by quantification of several metabolites in biological fluids. The aim of this review is to report the role of the laboratory in IEM diagnosis, highlighting the methods available at present and their advantages and limitations. In conclusion, the huge number of recognized IEMs strongly advises the implementation of new high- output technologies in the laboratories devoted to IEM diagnosis. Although these technologies offer a high diagnostic ability, routine analyses are still very important, as well as consideration of several variables involved in biological sample collection and disease expression that may lead to misdiagnosis of IEMs.

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Publicado

2008-10-07

Cómo citar

Artuch, R., Moreno, J., Puig, R., Quintana, M., Montero, R., Ormazábal, A., & Vilaseca, M. (2008). El laboratorio en el diagnóstico de las enfermedades raras. Anales Del Sistema Sanitario De Navarra, 31, 91–103. Recuperado a partir de https://recyt.fecyt.es/index.php/ASSN/article/view/1968

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