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dc.contributor.authorOner, Naci
dc.contributor.authorErtugrul, Turkan
dc.contributor.authorKayserili, Hulya
dc.contributor.authorNİŞLİ, Kemal
dc.date.accessioned2022-02-18T09:16:11Z
dc.date.available2022-02-18T09:16:11Z
dc.date.issued2008
dc.identifier.citationNİŞLİ K., Oner N., Kayserili H., Ertugrul T., "A case of Hennekam syndrome presenting with massive pericardial effusion", TURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY, cilt.36, sa.5, ss.325-328, 2008
dc.identifier.othervv_1032021
dc.identifier.otherav_2a68fb44-0cb7-493c-a433-92cced069b1b
dc.identifier.urihttp://hdl.handle.net/20.500.12627/176869
dc.description.abstractHennekam syndrome is an autosomal recessive disease characterized by intestinal lymphangiectasia accompanied by severe lymphedema of the limbs, genitalia, and face, and learning difficulties. A 38-month-old boy was admitted with breathing difficulty. He had facial abnormalities and preputial hyperplasia consistent with Hennekam syndrome. Lymphangiography showed lymphedema in the left eye and right foot. Teleradiography showed cardiomegaly and echocardiography showed massive pericardial effusion. He first underwent pericardiocentesis for the removal of pericardial effusion, but pericardial tube drainage was required upon recurrence of effusion. On the fifth day, the drain was removed because of significant decrease in the drainage.
dc.language.isoeng
dc.subjectKardiyoloji
dc.subjectCardiology and Cardiovascular Medicine
dc.subjectHealth Sciences
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.titleA case of Hennekam syndrome presenting with massive pericardial effusion
dc.typeMakale
dc.relation.journalTURK KARDIYOLOJI DERNEGI ARSIVI-ARCHIVES OF THE TURKISH SOCIETY OF CARDIOLOGY
dc.contributor.departmentİstanbul Teknik Üniversitesi , İstanbul Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü
dc.identifier.volume36
dc.identifier.issue5
dc.identifier.startpage325
dc.identifier.endpage328
dc.contributor.firstauthorID3375869


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