| Literature DB >> 17664775 |
A Dogra1, G S Bajwa, N Bajwa, S Khurana.
Abstract
A case of alkaptonuria, a rare autosomal recessive metabolic disorder is being reported. The patient presented with passage of dark coloured urine, cutaneous and scleral pigmentation and joint pains. The diagnosis was confirmed by the detection of homogentisic acid in the urine.Entities:
Year: 2001 PMID： 17664775
Source DB: PubMed Journal: Indian J Dermatol Venereol Leprol ISSN： 0378-6323 Impact factor: 2.545