Caffey disease, or infantile cortical hyperostosis, classically describes a self-limited
inflammatory disorder that presents in the infant with fussiness, focal swelling and …

Background Infantile cortical hyperostosis (ICH)/Caffey disease is an inflammatory
collagenopathy of infancy, manifested by subperiosteal bone hyperplasia. Genetically, ICH …

En dépit des taux élevés de mortalité infantile dans les populations du passé, les sujets
décédés en période périnatale ont longtemps été délaissés dans les travaux …

Caffey disease is characterized by massive subperiosteal new bone formation (usually
involving the diaphyses of the long bones as well as the ribs, mandible, scapulae, and …

We describe a rare case of monostotic infantile cortical hyperostosis (Caffey disease)
involving the left femur of an infant, who presented with recent onset left thigh swelling …

A previously healthy female infant was brought to the paediatrics outpatient department by
her mother reporting increased irritability and swelling behind her left shoulder …

Case Report Page 1 Vol 10 | Issue 7 | July 2023 Indian J Child Health 94 Case Report Case
report on Caffeys disease in an adolescent with a familial aspect Milind Kanjalkar1, Prachi …

A 2-weeks-old Saudi neonate was apparently well till the 10th day of life when a swelling of
the right groin was noted accompanied by irritability and fever, without history of trauma. On …

Caffey's disease or infantile cortical hyperostosis (ICH) was first reported in 1945 by Caffey
and Silverman. The disease is a rare and poorly understood disorder in infants …

Infantile cortical hyperostosis or Caffey disease is a rare genetic disorder caused by a
mutation in the collagen 1 gene. The mechanism of the disease has not yet been fully …