Friday 28 February 2014

Tyrosinemia Type I

Tyrosinemia

It is a hereditary illness categorized by high blood levels of the amino acid tyrosine, a structure block of most proteins. Tyrosinemia is triggered by the lack (deficiency) of one of the enzymes compulsory for the multi step procedure that breaks down tyrosine.


Symptoms
In the so-called acute form of the disease, irregularities seem in the first month of life can be noticed.

Diagnosis
This disorder can be complete by calculating the quantity of succinyl acetone in the urine or by an enzyme test on blood, liver or skin testers.
Treatment

Your baby’s doctors will effort with a metabolic doctor and dietitian to attention for your child. Enduringcure is usually wanted to avert kidney and liver difficulties.




1 comment:

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