Matches in SemOpenAlex for { <https://semopenalex.org/work/W2019352214> ?p ?o ?g. }
Showing items 1 to 63 of
63
with 100 items per page.
- W2019352214 endingPage "83" @default.
- W2019352214 startingPage "75" @default.
- W2019352214 abstract "Caffey-Silverman syndrome, or infantile hyperostosis, is a rare condition of unclear etiology and pathogenesis affecting the skeletal system and the surrounding soft tissues. It is characterized by indurated swelling of soft tissues and cortical bone hyperostosis. The changes are usually multiple and affect such parts as the mandible, scapulae, ribs, clavicles, and forearm and shank bones. When long bones are affected, the lesions are typically limited to shafts, with the sparing of meta- and epiphyses. The prognosis is usually good and, in most patients, the changes resolve spontaneously after several months to over a year, leaving no permanent sequelae. Caffey-Silverman syndrome needs to be distinguished from osteitis, for which it is most often mistaken. We present a case of an early form of Caffey-Silverman syndrome. The course of disease in this form is usually severe, with multifocal lesions, and the typical self-limiting regression is not complete. In our patient, a systemic musculoskeletal condition was already suspected following the detection of skeletal defects in a prenatal US examination. Physical and radiological work-up in the first weeks of life revealed the typical signs of congenital Caffey-Silverman syndrome. Several years of follow-up showed gradual regression of the bone deformities with persistent lower-extremity bowing. Due to a positive family history for Caffey-Silverman syndrome, the patient's pedigree was prepared. On the basis of the history data, existing radiographs and in- and outpatient medical records, Caffey-Silverman syndrome was confirmed in 10 family members. It was established that the cases of Caffey-Silverman syndrome in the patient's family were characterized by diverse phenotypic expression and different times of onset." @default.
- W2019352214 created "2016-06-24" @default.
- W2019352214 creator A5028442702 @default.
- W2019352214 creator A5031790625 @default.
- W2019352214 creator A5046519449 @default.
- W2019352214 creator A5067360030 @default.
- W2019352214 date "2012-02-29" @default.
- W2019352214 modified "2023-09-25" @default.
- W2019352214 title "Familial occurrence of Caffey-Silverman syndrome" @default.
- W2019352214 doi "https://doi.org/10.5604/15093492.976906" @default.
- W2019352214 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22408114" @default.
- W2019352214 hasPublicationYear "2012" @default.
- W2019352214 type Work @default.
- W2019352214 sameAs 2019352214 @default.
- W2019352214 citedByCount "1" @default.
- W2019352214 countsByYear W20193522142012 @default.
- W2019352214 crossrefType "journal-article" @default.
- W2019352214 hasAuthorship W2019352214A5028442702 @default.
- W2019352214 hasAuthorship W2019352214A5031790625 @default.
- W2019352214 hasAuthorship W2019352214A5046519449 @default.
- W2019352214 hasAuthorship W2019352214A5067360030 @default.
- W2019352214 hasConcept C105702510 @default.
- W2019352214 hasConcept C126322002 @default.
- W2019352214 hasConcept C137627325 @default.
- W2019352214 hasConcept C141071460 @default.
- W2019352214 hasConcept C142724271 @default.
- W2019352214 hasConcept C160306043 @default.
- W2019352214 hasConcept C2776260777 @default.
- W2019352214 hasConcept C2779782008 @default.
- W2019352214 hasConcept C3020110884 @default.
- W2019352214 hasConcept C71924100 @default.
- W2019352214 hasConceptScore W2019352214C105702510 @default.
- W2019352214 hasConceptScore W2019352214C126322002 @default.
- W2019352214 hasConceptScore W2019352214C137627325 @default.
- W2019352214 hasConceptScore W2019352214C141071460 @default.
- W2019352214 hasConceptScore W2019352214C142724271 @default.
- W2019352214 hasConceptScore W2019352214C160306043 @default.
- W2019352214 hasConceptScore W2019352214C2776260777 @default.
- W2019352214 hasConceptScore W2019352214C2779782008 @default.
- W2019352214 hasConceptScore W2019352214C3020110884 @default.
- W2019352214 hasConceptScore W2019352214C71924100 @default.
- W2019352214 hasIssue "1" @default.
- W2019352214 hasLocation W20193522141 @default.
- W2019352214 hasLocation W20193522142 @default.
- W2019352214 hasOpenAccess W2019352214 @default.
- W2019352214 hasPrimaryLocation W20193522141 @default.
- W2019352214 hasRelatedWork W1495786304 @default.
- W2019352214 hasRelatedWork W1993722118 @default.
- W2019352214 hasRelatedWork W2025596629 @default.
- W2019352214 hasRelatedWork W2077729089 @default.
- W2019352214 hasRelatedWork W2106988518 @default.
- W2019352214 hasRelatedWork W2219786428 @default.
- W2019352214 hasRelatedWork W2410539510 @default.
- W2019352214 hasRelatedWork W2581699428 @default.
- W2019352214 hasRelatedWork W3002986063 @default.
- W2019352214 hasRelatedWork W4322705554 @default.
- W2019352214 hasVolume "14" @default.
- W2019352214 isParatext "false" @default.
- W2019352214 isRetracted "false" @default.
- W2019352214 magId "2019352214" @default.
- W2019352214 workType "article" @default.