The de Barsy Syndrome

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dc.contributor.authorArazi, Mehmet
dc.contributor.authorKapıcıoğlu, M. I. S.
dc.contributor.authorMutlu, M.
dc.date.accessioned2020-03-26T16:37:27Z
dc.date.available2020-03-26T16:37:27Z
dc.date.issued2001
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractWe report a child with de Barsy syndrome, which is a very rare, genetically transmitted clinical entity associated with mental and growth retardation, severe cutis laxa, joint laxity and various ocular and skeletal system findings. The patient was operated to treat her orthopedic disabilities. Typical findings of this case with eight-year follow-up beginning from birth are described and compared with previously reported cases. The main aim of this paper was to describe the diagnostic and therapeutic difficulties of this rarely encountered syndrome.en_US
dc.identifier.citationArazi, M., Kapıcıoğlu, M. I. S., Mutlu, M., (2001). The de Barsy Syndrome. Turkish Journal of Pediatrics, 43(1), 79-84.
dc.identifier.endpage84en_US
dc.identifier.issn0041-4301en_US
dc.identifier.issue1en_US
dc.identifier.pmid11297166en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage79en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/17624
dc.identifier.volume43en_US
dc.identifier.wosWOS:000167689400016en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherTURKISH J PEDIATRICSen_US
dc.relation.ispartofTurkish Journal of Pediatricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectde Barsy syndromeen_US
dc.subjecthypermobilityen_US
dc.subjectelastinen_US
dc.subjectcutis laxaen_US
dc.subjectchildrenen_US
dc.titleThe de Barsy Syndromeen_US
dc.typeArticleen_US

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