Alkaptonuria: A case report

Alkaptonuria is a rare inborn error of metabolism with here autosomal recessive inheritance with a mutation in homogentisate 1,2-dioxygenase.It results in accumulation of homogentisic acid in connective tissues (ochronosis).Most common ocular manifestations are bluish-black discoloration of the conjunctiva, cornea, and sclera.In this case report, a

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