Causas de Alcaptonuria: factores genéticos y ambientales explicados y revisados con fuentes médicas, más la perspectiva de los pacientes.
Original
Alkaptonuria is a rare inherited genetic disorder in which the body cannot process the amino acids phenylalanine and tyrosine, which occur in protein. It is caused by a mutation in the HGD gene for the enzyme homogentisate 1,2-dioxygenase.