Alkaptonuria.
Indian J Dermatol Venereol Leprol
;
2001 Sep-Oct; 67(5): 271-2
Article
in English
| IMSEAR
| ID: sea-53051
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.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Language:
English
Journal:
Indian J Dermatol Venereol Leprol
Year:
2001
Type:
Article
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