Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. [[Alkaptonuria]] is a rare inherited genetic disorder in which the body cannot process the [[aminoacid]]s [[phenylalanine]] and [[tyrosine]], which occur in [[protein]]. It is caused by a mutation in the HGD gene for the enzyme homogentisate 1,2-dioxygenase (EC 1.13.11.5); if a person inherits abnormal copies from each parent (it is a [[recessive]] condition), the body accumulates an intermediate substance called [[homogentisic acid]] in the blood and tissues. Homogentisic acid and its oxidized form alkapton are excreted in the urine, giving it an unusually dark color. The accumulating homogentisic acid causes damage to cartilage ([[ochronosis]], leading to osteoarthritis) and heart valves, as well as precipitating as kidney stones and stones in other organs. homogentisic_acid.txt Last modified: 2024/06/07 02:59by 127.0.0.1