[Studies on diaphyseal cortical hyperostosis in infant; familial Caffey's syndrome].
D001847:Bone Diseases; D003966:Camurati-Engelmann Syndrome; D016537:Gangliosidosis, GM1; D006801:Humans; D006958:Hyperostosis, Cortical, Congenital; D007223:Infant
BONES/diseases
Contributo alla conoscenza delle iperostosi corticali diafisarie del lattante; sindrome di Caffey a carattere familiare.