Ici vous pouvez voir affichés quelques unes des causes de la Alcaptonurie selon les personnes ayant de l'expertise en Alcaptonurie
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.