Which of the following inborn error of metabolism has porphyria like clinical features?
Correct Answer: Tyrosinemia type I
Description: Succinylacetone accumulates in hereditary tyrosinemia type I (fumarylacetoacetate hydrolase deficiency). Succinylacetone is structurally similar to ALA and inhibits ALA dehydratase leading to porphyria like features.
Category:
Biochemistry
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