Browsing Research Publications by Subject "Pyle disease (OMIM 265900)"
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Pyle metaphyseal dysplasia in an African child: Case report and review of the literature
(Health & Medical Publishing Group, 2016)Pyle disease (OMIM 265900), also known as metaphyseal dysplasia, is a rare autosomal recessive disorder with no known gene mutation. We report a case of Pyle disease in a 7-year-old African boy of mixed ancestry who ...