This HTML5 document contains 23 embedded RDF statements represented using HTML+Microdata notation.

The embedded RDF content will be recognized by any processor of HTML5 Microdata.

PrefixNamespace IRI
vivohttp://vivoweb.org/ontology/core#
dctermshttp://purl.org/dc/terms/
n4http://hub.abes.fr/referentiel/bmjarticlecategories/subject/
n2http://hub.abes.fr/bmj/periodical/bmjcasereports/2012/volume_2012/issue_2012/B354D643B3180773E053120B220ACE76/
n9http://hub.abes.fr/bmj/periodical/bmjcasereports/2012/volume_2012/issue_2012/B354D643B3180773E053120B220ACE76/authorship/
n15http://hub.abes.fr/bmj/periodical/bmjcasereports/2012/volume_2012/issue_2012/
bibohttp://purl.org/ontology/bibo/
n10http://hub.abes.fr/bmj/periodical/bmjcasereports/
rdachttp://rdaregistry.info/Elements/c/
hubhttp://hub.abes.fr/namespace/
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n14http://hub.abes.fr/bmj/periodical/bmjcasereports/2012/volume_2012/issue_2012/B354D643B3180773E053120B220ACE76/m/
n7http://hub.abes.fr/bmj/periodical/articletype/
rdawhttp://rdaregistry.info/Elements/w/
n5http://hub.abes.fr/referentiel/hwpjournalcoll/subject/
xsdhhttp://www.w3.org/2001/XMLSchema#
Subject Item
n2:w
rdf:type
bibo:Article rdac:C10001
dcterms:isPartOf
n15:w
dcterms:subject
n4:male n5:orthopaedics n4:neonate n5:paediatrics n5:raredisease n4:europewest n4:raredisease n5:genetics n4:black
dcterms:title
Caffey disease in neonatal period: the importance of the family!
rdaw:P10072
n14:print n14:web
vivo:relatedBy
n9:2 n9:1 n9:3 n9:4
dcterms:abstract
A male newborn was apparently well until his second day of life, when increased irritability and a swelling in his right leg were noted. He was rooming-in with his mother since birth. On examination, a mass on the anterior surface of the right leg was noticed. The mass was firm, elongated, ill-defined, unmovable and painful at palpation. No overlying skin changes were seen. The newborn had a family history of neonatal bone swelling with resolution before the age of 2. Subsequent images showed hyperostosis in the diaphysis of the right tibia. After exclusion of other conditions such as trauma, osteomyelitis and congenital syphilis, the involvement of the tibial diaphysis, sparing the epiphyses and the benign course of the disease in family history, were indicative of Caffey disease. The genetic study confirmed this diagnosis. Caffey disease, although rare, should not be overlooked in the diagnostic approach to childhood bone swelling.
hub:articleType
n7:casereport
hub:publisher-id
bcr-2012-006996
hub:isPartOfThisJournal
n10:w