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Primary lymphoedema at an unusual location triggered by nephrotic syndrome

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dc.contributor.author Tabel, Yılmaz
dc.contributor.author Mungan, İlke
dc.contributor.author Sığırcı, Ahmet
dc.contributor.author Güngör, Serdal
dc.date.accessioned 2017-06-20T12:29:33Z
dc.date.available 2017-06-20T12:29:33Z
dc.date.issued 2009
dc.identifier.citation Tabel, Y. Mungan, İ. Sığırcı, A. Güngör, S. (2009). Primary lymphoedema at an unusual location triggered by nephrotic syndrome. Ann Acad Med Singapore. 38, 636-638. tr_TR
dc.identifier.uri http://hdl.handle.net/11616/7136
dc.description.abstract Introduction: Lymphoedema results from impaired lymphatic transport leading to the pathologic accumulation of protein-rich lymphatic fl uid in the interstitial space, most commonly in the extremities. Primary lymphoedema, a developmental abnormality of the lymphatic system, may become evident later in life when a triggering event exceeds the capacity of normal lymphatic fl ow. Clinical Picture: We present a 3-year-old nephrotic syndrome patient with an unusual localisation for primary lymphoedema. Treatment and Outcome: The patient was treated with conservative approach and she was cured. Conclusion: In this particular case, lymphoedema developed at an unusual localisation, which has not been recorded before. tr_TR
dc.language.iso eng tr_TR
dc.publisher Ann Acad Med Singapore tr_TR
dc.rights info:eu-repo/semantics/openAccess tr_TR
dc.subject Childhood tr_TR
dc.subject Conservative treatment tr_TR
dc.title Primary lymphoedema at an unusual location triggered by nephrotic syndrome tr_TR
dc.type article tr_TR
dc.relation.journal Ann Acad Med Singapore tr_TR
dc.contributor.department İnönü Üniversitesi tr_TR
dc.contributor.authorID 7768 tr_TR
dc.identifier.volume 38 tr_TR
dc.identifier.startpage 636 tr_TR
dc.identifier.endpage 638 tr_TR


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