Association of Primum-Type Atrial Septal Defect and Patent Foramen Ovale in a Patient with Holt-Oram Syndrome

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dc.contributor.authorKaya, Hasan
dc.contributor.authorYavuz, Celal
dc.contributor.authorErtaş, Faruk
dc.contributor.authorÇoşkun, Mehmet Sait
dc.date.accessioned2024-04-24T19:11:36Z
dc.date.available2024-04-24T19:11:36Z
dc.date.issued2019
dc.departmentDicle Üniversitesien_US
dc.description.abstractA 49-year-old woman with dwarfism reported signs of shortness of breath. A physical examination of the patient revealed congenital deformities in the hands and feet (Figure 1). Radiographs showed that the extremities of both her hands had metatarsal polydactyly; moreover, with her feet seem to have epiphyseal dysplasia and polysyndactyly were determined (Figure 2). Telecardiography showed cardiomegaly, and electrocardiography showed rightaxial deviation and right ventricular hypertrophyen_US
dc.identifier.doi10.5578/khj.68335
dc.identifier.endpage142en_US
dc.identifier.issn2149-2980
dc.identifier.issue2en_US
dc.identifier.startpage141en_US
dc.identifier.trdizinid342604
dc.identifier.urihttps://doi.org/10.5578/khj.68335
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/342604
dc.identifier.urihttps://hdl.handle.net/11468/28105
dc.identifier.volume22en_US
dc.indekslendigikaynakTR-Dizin
dc.language.isoenen_US
dc.relation.ispartofKoşuyolu Heart Journal
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleAssociation of Primum-Type Atrial Septal Defect and Patent Foramen Ovale in a Patient with Holt-Oram Syndromeen_US
dc.titleAssociation of Primum-Type Atrial Septal Defect and Patent Foramen Ovale in a Patient with Holt-Oram Syndrome
dc.typeOtheren_US

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