Expain what is Phenylalanine-Tyrosine Disorders

Reference no: EM133700621

¦ 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 aminotransferase.

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

Reference no: EM133700621

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