Sridhar F K, Mukha R P, Kumar S, Kekre N S
Department of Urology, Christian Medical College and Hospital, Vellore, Tamil Nadu, India.
Indian J Urol. 2012 Apr;28(2):219-21. doi: 10.4103/0970-1591.98474.
Alkaptonuria is a rare tyrosine metabolic disorder. A deficiency of homogentisic acid oxidase leads to accumulation of homogentisic acid in the body. Dark-colored urine, cutaneous pigmentations and musculoskeletal deformities are characteristic features. Storage and voiding lower urinary tract symptoms due to prostatic calculi is a rare presentation.
黑尿症是一种罕见的酪氨酸代谢紊乱疾病。尿黑酸氧化酶缺乏会导致尿黑酸在体内蓄积。深色尿液、皮肤色素沉着和肌肉骨骼畸形是其特征性表现。因前列腺结石导致的下尿路储尿和排尿症状是一种罕见的表现。