Hyperostosis

È il momento di un buon Caffey

Del Rizzo I, Zago A, D’Agostin M, Gortani G, Colin G, Barbi E, Magnolato A.

2024/9 — pag. 594-596 — DOI

It is a rare genetic condition characterized by bone proliferation and cortical thickening due to a genetic mutation. The infantile form appears in the first months of life, with subperiosteal bone deposits, and generally resolves by the age of two w...

Displasia ossea con scarsa crescita

A. Trombetta

2020/10 — pag. 257-258 — DOI

A case of a short girl affected by multiple familial osteochondrosis (MFO) is described. The Author underlines the need of a strict, long term clinical monitoring in all MFO children and in their affected parents because of a significantly increased ...

L’iperostosi corticale infantile (malattia di Caffey)

M. Minute, P. Moras, E. Lelio

2020/4 — pag. 255-257

Un ditone spropositato

C. Gussoni

2012/8

Esostosi della testa fibulare e compressionedel nervo peroneale: descrizione di un casoin un adolescente

R. Fagioli, S. Brachi, G. Borsari, S. Rinieri, E. Gastaldo

2008/7 — pag. 463-464

The peroneal nerve is frequently involved in cases of lesions or entrapment in the lower limb. In literature, only few cases have been reported on peroneal nerve compression by a benign bone growth, such as exostosis. We report the case of a 13 y...

Esostosi della testa fibulare e compressione del nervo peroneale: descrizione di un caso in un adolescente

R. Fagioli, S. Brachi, G. Borsari, S. Rinieri, E. Gastaldo

2008/7

Osteofiti

G. Maranzana

1999/3