Alkaptonuria
A case of alkaptonuria, a rare disorder with autosomal recessive inheritance, is reported here. The patient had palmar pigmentation in addition to the usual features of alkaptonuria.
Main Authors: | G K Tharini, Vidhya Ravindran, N Hema, D Prabhavathy, B Parveen |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2011-01-01
|
Series: | Indian Journal of Dermatology |
Subjects: | |
Online Access: | http://www.e-ijd.org/article.asp?issn=0019-5154;year=2011;volume=56;issue=2;spage=194;epage=196;aulast=Tharini |
Similar Items
-
Alkaptonuria: Case report
by: Swapna S Khatu, et al.
Published: (2015-01-01) -
Alkaptonuria and Ochronosis – Experience From Slovakia
by: Rovenský J., et al.
Published: (2014-08-01) -
Alkaptonuria in a 6 Year Old Patient: Case Report
by: Vikas Sharma, et al.
Published: (2015-11-01) -
Demographic, Phenotypic and Genotypic Features of Alkaptonuria Patients: A Single Centre Experience
by: Sebile Kılavuz, et al.
Published: (2018-03-01) -
A case report of pregnancy in untreated alkaptonuria – Focus on urinary tissue remodelling markers
by: L.R. Ranganath, et al.
Published: (2021-06-01)