Chapman T et al: Radiographic overlap of recurrent Caffey disease and chronic recurrent multifocal osteomyelitis (CRMO) with considerations of molecular origins. Pediatr Radiol. 50(5):618-27, 2020
Hoen N et al: Prenatal Caffey disease (prenatal cortical hyperostosis): severe forms with favorable outcome. Prenat Diagn. 35(4):409-11, 2015
Kitaoka T et al: Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature. Eur J Pediatr. 173(6):799-804, 2014
Nistala H et al: Caffey disease: new perspectives on old questions. Bone. 60:246-51, 2014
Newberg AH et al: Familial infantile cortical hyperostosis: an update. AJR Am J Roentgenol. 137(1):93-6, 1981
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Chapman T et al: Radiographic overlap of recurrent Caffey disease and chronic recurrent multifocal osteomyelitis (CRMO) with considerations of molecular origins. Pediatr Radiol. 50(5):618-27, 2020
Hoen N et al: Prenatal Caffey disease (prenatal cortical hyperostosis): severe forms with favorable outcome. Prenat Diagn. 35(4):409-11, 2015
Kitaoka T et al: Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature. Eur J Pediatr. 173(6):799-804, 2014
Nistala H et al: Caffey disease: new perspectives on old questions. Bone. 60:246-51, 2014
Newberg AH et al: Familial infantile cortical hyperostosis: an update. AJR Am J Roentgenol. 137(1):93-6, 1981
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