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Title: The Tel Hashomer camptodactyly syndrome: report of a new case and review of the literature. Author: Pagnan NA, Gollop TR, Lederman H. Journal: Am J Med Genet; 1988 Feb; 29(2):411-7. PubMed ID: 3281460. Abstract: We report on a new case of Tel Hashomer camptodactyly syndrome and review the literature. This syndrome is characterized by skeletal dysplasia, muscle hypoplasia, camptodactyly, and abnormal dermatoglyphics. The inheritance is autosomal recessive with probable partial expression in the heterozygote.[Abstract] [Full Text] [Related] [New Search]