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Craniofacial, dental, and molecular features of Pyle disease in a South African child
(Springer Nature, 2022)
Pyle Disease (PD), or familial metaphyseal dysplasia [OMIM 265900], is a rare autosomal recessive condition
leading to widened metaphyses of long bones and cortical bone thinning and genu valgum. We detail the oro-dental ...