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1. LEOPARD syndrome: Report of a case

A Ramazanpour; H Babaei

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 More