Expain what is tyrosinemia

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Reference no: EM133804550

Question: Expain what is Tyrosinemia - Inherited disorder that leads to tyrosine accumulation. - Loss/defect in enzyme that catabolizes tyrosine in liver

Type I- most severe (decreased levels of fumarylacetoacetate hydrolase)

Type II- (rare) deficiency of tyrosine amino transferase. Your Writing Experts Are Ready - Hire Now!

Type III- (very rare) Deficiency of 4-hydroxyphenylpyruvate dioxygenase (build up of tyrosine) failure to thrive, jaundice, cabbage-like odor, nose bleeds !liver & kidney failure, neuropathy & hepatic tumors Excessive tearing, photophobia, eye pain, lesions and mental retardation. mild retardation, seizures and intermittent ataxia.

Reference no: EM133804550

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Expain what is tyrosinemia : Deficiency of 4-hydroxyphenylpyruvate dioxygenase (build up of tyrosine) failure to thrive, jaundice, cabbage-like odor, nose bleeds

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