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pro vyhledávání: '"Sameen Farah"'
Autor:
Qurashi, Taha Ashraf, Bhat, Gulzar Ahmad, Khan, Mosin Saleem, Rasool, Roohi, Sameen, Farah, Hassan, Iffat, Mudassar, Syed
Publikováno v:
In Clinical Immunology August 2021 229
Publikováno v:
Indian Journal of Dermatology, Vol 52, Iss 1, Pp 53-55 (2007)
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 prolida
Externí odkaz:
https://doaj.org/article/69068aa7765e40a08b351ec2c85cba2f