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An unusual association of TAR syndrome with esophageal atresia: A variant?

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dc.creator EREN, Esin
dc.creator TUNC, B
dc.creator Savas, Mustafa Çağrı
dc.creator Buyukyavus, Behçet İlker
dc.creator OZGUNER, IF
dc.date 2005-08-31T21:00:00Z
dc.date.accessioned 2020-10-06T10:49:28Z
dc.date.available 2020-10-06T10:49:28Z
dc.identifier 96ce38ff-da7b-4aa1-babc-c0acde47b48e
dc.identifier 10.1080/08880010591002332
dc.identifier https://avesis.sdu.edu.tr/publication/details/96ce38ff-da7b-4aa1-babc-c0acde47b48e/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/66954
dc.description Thrombocytopenia and absent radii (TAR) syndrome is a rare disorder. It may be associated with for example, as cardiovascular, genitourinary, gastrointestinal, skeletal, neurological, ophthalmic, and facial anomalies. Esophageal atresia is also a rare anomaly associated with genitourinary, skeletal, and cardiovascular anomalies, among others. Here, the authors present a child with TAR syndrome and esophageal atresia with tracheoesophageal fistula. This association has been reported in only one other case in literature.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title An unusual association of TAR syndrome with esophageal atresia: A variant?
dc.type info:eu-repo/semantics/article


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