Indian Journal of Dermatology
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CASE REPORT
Year : 2007  |  Volume : 52  |  Issue : 1  |  Page : 53-55

Prolidase deficiency


Department of Dermatology, STD, Leprosy and Biochemistry, Govt. Medical College, Srinagar, India

Correspondence Address:
Taseer Ahmed Bhatt
R/O:-Shabeer Manzil, Rajbagh Extension, Srinagar, Kashmir - 190 008 (J and K)
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0019-5154.31927

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Prolidase deficiency is a rare inborn disorder of collagen metabolism characterized by chronic recurrent skin ulceration. A seven-year-old girl and her younger sibling with clinical features and laboratory criteria fulfilling the diagnosis of prolidase deficiency are presented in view of rarity of the condition.


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