Publication:
Caffey’s Disease (Infantile Cortical Hyperostosis)

creativeworkseries.issnISSN 1990-7974 eISSN 1990-7982
dc.contributor.authorParia, Pradipprava
dc.contributor.authorHalder, Ramesh Chandra
dc.contributor.authorGhosh, Sibarjun
dc.date.accessioned2026-03-17T11:13:25Z
dc.date.available2026-03-17T11:13:25Z
dc.date.issued2015
dc.descriptionPradipprava Paria Department of Paediatric Medicine, RG Kar Medical College, Kolkata Ramesh Chandra Halder Department of Paediatric Medicine, RG Kar Medical College, Kolkata Sibarjun Ghosh Department of Paediatric Medicine, RG Kar Medical College, Kolkata
dc.description.abstractAbstract: Caffey's disease is a rare, self limiting condition of infancy. Most commonly mandible, clavicle and ulna are affected leading to inflammation of periosteum and overlying soft tissue. We here present an 1 year 3 month old girl with features of Caffey's disease.
dc.identifierhttps://doi.org/10.3126/jnps.v35i3.13080
dc.identifier.urihttps://hdl.handle.net/20.500.14572/5211
dc.language.isoen_US
dc.publisherNepal Paediatric Society (JNPS)
dc.subjectCaffey disease
dc.subjectcortical hyperostosis
dc.subjectNSAIDS
dc.titleCaffey’s Disease (Infantile Cortical Hyperostosis)
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage313
oaire.citation.startPage312
relation.isJournalIssueOfPublicationddb30430-3a07-48b1-8970-c896f031201d
relation.isJournalIssueOfPublication.latestForDiscoveryddb30430-3a07-48b1-8970-c896f031201d
relation.isJournalOfPublication6f9be05c-05a9-4a3e-a5b5-a19a15ab042c

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