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Author = A Ramazanpour
Number of Articles: 2
LEOPARD syndrome: Report of a case
Volume 6, Issue 4 , 2003, , Pages 51-54
Abstract
LEOPARD syndrome is an autosomal dominant hereditary disease, which is characterized with cutaneous pigmented patches, electrocardiographic changes, ocular hypertelorism, retarded growth, pulmonic stenosis, genital abnormalities and congenital deafness. The gene of this disease have high penetrance but ... Read MoreAssociation of Porokeratosis, Vitiligo, Lichen Sclerosus et Atrophicus and Lichen Planus: A case report
Volume 5, Issue 4 , 2002, , Pages 44-47