[Infantile cortical hyperostosis (Caffey-Smith syndrome)].
D001847:Bone Diseases; D016537:Gangliosidosis, GM1; D006801:Humans; D006958:Hyperostosis, Cortical, Congenital
BONES/diseases
Contributo allo studio dell'iperostosi corticale infantile: (sindrome di Caffey Smith).