Neurological crisis in hereditary tyrosinaemia
PDF (Español (España))

Keywords

Type I Tyrosinaemia
Neurological Crisis
Children
Neurology
Metabolism Inborn Errors
Amino Acid Metabolism

How to Cite

1.
Wenzel A. MS, Scheuch R. K, Krause H. S. Neurological crisis in hereditary tyrosinaemia. Andes pediatr [Internet]. 2003 Jun. 19 [cited 2025 Sep. 12];74(6):604-8. Available from: https://andespediatrica.cl/index.php/rchped/article/view/2010

Abstract

Type I tyrosinaemia results from an inborn error in the final step of tyrosine metabolism. Clinical manifestations are diverse and worsen with the development of neurological crises. The aim of this article is to report the clinical course of a child with this disease who developed a flaccid paralysis with respiratory failure and needed mechanical ventilation.
PDF (Español (España))
Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

Copyright (c) 2003 Revista Chilena de Pediatría