TYRo Concept

The dietary management consists of a diet low in Tyrosine and its precursor Phenylalanine (i.e. low in native protein) with addition of amino acids supplements free from these amino acids.

Tyrosinemia

Tyrosinemia is an inherited rare disorder in metabolism of the amino acid Tyrosine. There are several types of Tyrosinemia, caused by different enzyme defects. If not treated, this condition leads to an accumulation of Tyrosine and Phenylalanine, as well as to formation of toxic metabolites in all body fluids. Depending on the type of the disorder, this can result in severe irreversible physical damages and finally death.

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COMIDAMED

Dr. Schär AG 


Winkelau 9
I - 39014 Burgstall / Postal


Tel. +39 0473 293 300
Fax +39 0473 293 399
info.it@drschaer.com

 

 

COMIDACLOUD

Aminosäurenmischung | diätetische Behandlung von Phenylketonurie | erstes Lebensjahr | Erwachsene | glutenfrei | HPA | Hyperphenylalaninämie | Jugendliche | Kinder | Kleinkinder | Kohlenhydrate | Mineralstoffe | phenylalaninfreie | Proteinsupplemente | Phenylketonurie | PKU | Schwangere |Spurenelemente | Säuglinge | Vitamine

COMIDATAGS

Germany | Entwicklung | Herstellung | spezielle Ernährung | medizinisch | Nährstoffe | Rosbach |