E' il momento di un buon Caffey
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 without sequelae.
Authors
- Martina D’Agostin (ORCID: https://orcid.org/0000-0002-7801-2883)
- Egidio Barbi (ORCID: https://orcid.org/0000-0002-6343-846X)
- Giulia Colin
- Andrea Magnolato (ORCID: https://orcid.org/0000-0002-5099-6526)
- Irene Del Rizzo (ORCID: https://orcid.org/0000-0002-2370-0021)
- Giulia Gortani (ORCID: https://orcid.org/0000-0002-2218-490X)
- Alessandro Zago
Institutions
- IRCCS Materno Infantile Burlo Garofolo (IT)
Publication Details
- Journal
- Medico e Bambino
- Published
- 2024-11-07
- DOI
- https://doi.org/10.53126/meb43596
- Primary Topic
- Diverse Academic Research Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00