Work

Tirosinemia hereditaria tipo I. A propósito de dos observaciones

Year: 1997

Type: article

Abstract: Two cases of type I hereditary tyrosinemia are presented. One of them died during a sepsis before beginnning a dietetic treatment; the other one, after having undergone a low in tirosine and fenilalanine diet from the age of 2 months, needed a liver transplant at the age of 7 months because of a severe hepatocelular failure and now evolving satisfactorily, after 5 years since the diagnostic was made.

Source: Boletín de Pediatría

Authors: Grande, A., Martín, M., Nava, E., García Fernández, M., Terceiro, O., Santamartina, V., González, P.

Institution: Complejo Hospitalario de Salamanca

Language: Spanish

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: hybrid

OpenAlex ID: W7217927733

FWCI:

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Related to: 10