CASE REPORT |
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Year : 2016 | Volume
: 3
| Issue : 1 | Page : 49-51 |
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Palmar pigmentation: An unusual presentation of alkaptonuria
H. V. S. Naveen Kumar, C Natraj Hiremath, N Bhuvanaa Sree, A Vijaya Mohan Rao
Department of Dermatology, Venereology and Leprosy, Narayana Medical College, Nellore, Andhra Pradesh, India
Correspondence Address:
Dr. H. V. S. Naveen Kumar Flat No: 201, H. No: 1-1-524, R. R. Arcade, Gandhinagar, Hyderabad, Telangana - 500 080 India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/2349-5847.184245
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Alkaptonuria (AKU) is a rare inherited autosomal recessive metabolic disorder, caused by the deficiency of homogentisic acid oxidase enzyme. Herein, we are reporting a case of AKU with bilaterally symmetrical palmar pigmentation and skeletal involvement. Histopathological examination revealed ochre colored pigment in the dermis whereas roentgenogram of the lumbar spine showed typical calcification of the intervertebral discs. |
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