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

Alkaptonuria

Alka Dogra, GS Bajwa, Navjot Bajwa, Shallu Khurana 
 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

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.


How to cite this article:
Dogra A, Bajwa G S, Bajwa N, Khurana S. Alkaptonuria.Indian J Dermatol Venereol Leprol 2001;67:271-272


How to cite this URL:
Dogra A, Bajwa G S, Bajwa N, Khurana S. Alkaptonuria. Indian J Dermatol Venereol Leprol [serial online] 2001 [cited 2019 Aug 22 ];67:271-272
Available from: http://www.ijdvl.com/article.asp?issn=0378-6323;year=2001;volume=67;issue=5;spage=271;epage=272;aulast=Dogra;type=0


 

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