COL1A1 gene mutation
1 articolo — 2020-2020
RI
Casi indimenticabili
L’iperostosi corticale infantile (malattia di Caffey)
M. Minute, P. Moras, E. Lelio
2020/4 — pag. 255-257
Argomenti correlati
Diagnosis, Differential (264)
Kawasaki disease (95)
Malattia di Kawasaki (79)
Osteomyelitis (73)
Osteomielite (44)
Bone Diseases, Developmental (12)
Periosteum (6)
Caffey disease (3)
Infantile cortical hyperostosis (3)
Complicated pneumonia (3)
Malattia di Caffey (3)
Polmonite complicata (3)
Iperostosi corticale infantile (2)
Hyperostosis, Cortical, Congenital (2)
Collagen Type I (2)
periosteal thickening (1)
neonatal bone dysplasia (1)
ispessimento periostale (1)
gene COL1A1 (1)
displasia ossea neonatale (1)