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Case Reports
. 2025 Oct;61(10):1699-1701.
doi: 10.1111/jpc.70185. Epub 2025 Sep 3.

A Newborn With Mandibular Swelling and Tibial Lumps

Affiliations
Case Reports

A Newborn With Mandibular Swelling and Tibial Lumps

Irene Del Rizzo et al. J Paediatr Child Health. 2025 Oct.
No abstract available

Keywords: caffey disease; mandibular swelling; rare diseases; tibial lumps.

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References

    1. R. C. Gensure, O. Mäkitie, C. Barclay, et al., “A Novel COL1A1 Mutation in Infantile Cortical Hyperostosis (Caffey Disease) Expands the Spectrum of Collagen‐Related Disorders,” Journal of Clinical Investigation 115 (2005): 1250–1257.
    1. A. K. Maclachlan, J. W. Gerrard, C. S. Houston, and E. J. Ives, “Familial Infantile Cortical Hyperosteosis in a Large Canadian Family,” Canadian Medical Association Journal 130 (1984): 1172–1174.
    1. A. R. Prior, O. Moldovan, A. Azevedo, and C. Moniz, “Caffey Disease in Neonatal Period: The Importance of the Family!,” BML Case Reports 2012 (2012): bcr2012006996, https://doi.org/10.1136/bcr‐2012‐006996.
    1. T. Chapman, S. J. Menashe, and B. H. Taragin, “Radiographic Overlap of Recurrent Caffey Disease and Chronic Recurrent Multifocal Osteomyelitis (CRMO) With Considerations of Molecular Origins,” Pediatric Radiology 50 (2020): 618–627, https://doi.org/10.1007/s00247‐019‐04590‐3.
    1. K. Suphapeetiporn, S. Tongkobpetch, A. Mahayosnond, and V. Shotelersuk, “Expanding the Phenotypic Spectrum of Caffey Disease,” Clinical Genetics 71 (2007): 280–284.

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