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 CASE REPORT
Year : 2001  |  Volume : 67  |  Issue : 5  |  Page : 271--272

Alkaptonuria


Department of Dermatology, Dayanand Medical College and Hospital, Ludhiana (Punjab), India

Correspondence Address:
Alka Dogra
Department of Dermatology, Dayanand Medical College and Hospital, Ludhiana (Punjab)
India
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Source of Support: None, Conflict of Interest: None


PMID: 17664775

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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.






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Online since 15th March '04
Published by Wolters Kluwer - Medknow