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Updated: Aug 9, 2026

High-throughput Screening for Protein-based Inheritance in S. cerevisiae
Published on: August 8, 2017
[Sepsis, as the presenting form of hereditary tyrosinemia type I]
J Iglesias Niubo1, E Riudor Taravilla, A R Goma Brufau
1Servicio de Pediatría de la Clínica Infantil de la Ciudad Sanitaria Vall d'Hebrón, Barcelona.
Abstract:
A case of hereditary tyrosinemia type I with a septic onset is reported. Diagnosis was established by the urinary presence of succinylacetone (SA) and deficiency in fumarylacetoacetate hydrolase (FAAH) in a culture of fibroblasts. Response to treatment with a diet in which the aminoacids phenylalanine, tyrosine and methionine were restricted is commented upon.
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