Ehlers-Danlos syndrome: A case report

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dc.contributor.authorTasdemir N.
dc.contributor.authorSarac A.J.
dc.contributor.authorTombul T.
dc.contributor.authorErdogan F.
dc.contributor.authorAtaoglu S.
dc.contributor.authorCevik R.
dc.date.accessioned2024-04-24T17:58:54Z
dc.date.available2024-04-24T17:58:54Z
dc.date.issued1996
dc.departmentDicle Üniversitesien_US
dc.description.abstractEhlers-Danlos syndrome a rare disease, it is inherited as an autosomal dominant trait. Clinically the skin is hyperextensible, fragile and brittle and bruises easily. The joints are hyperextensible and can be pulled apart longitudinally to an abnormal degree. We presented a patient who was complaining from muscle pain, muscle weakness and especially hyperextensible metacorpophalangeal and interphalangeal joints. We described that he has been suffering from EDS type II which is a less severe form of EDS. Then we reviewed this rare syndrome from the literature.en_US
dc.identifier.endpage198en_US
dc.identifier.issn1300-6614
dc.identifier.issue4en_US
dc.identifier.scopus2-s2.0-0030427293en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage194en_US
dc.identifier.urihttps://hdl.handle.net/11468/24150
dc.identifier.volume20en_US
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.relation.ispartofFizik Tedavi Rehabilitasyon Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectEhlers-Danlos Syndromeen_US
dc.subjectHyperextensibilityen_US
dc.titleEhlers-Danlos syndrome: A case reporten_US
dc.title.alternativeEhlers-Danlos sendromu. (Olgu sunumu)en_US
dc.typeArticleen_US

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