CASE REPORT: FROM MONKEYPOX PHARYNGITIS TO MYOPERICARDITIS AND ATYPICAL SKIN LESIONS





Alkaptonuria: A case report

Alkaptonuria is a rare cubs foam finger inborn error of metabolism with 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 better waters xl7000 manifestations are bluish-black discoloration of the conjunctiva, cornea,

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