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dc.contributor.authorSaç, Rukiye
dc.contributor.authorGüveloğlu, Mine
dc.contributor.authorBostancı, İlknur
dc.contributor.authorTazegül, Aysu
dc.contributor.authorDallar, Yıldız
dc.date.accessioned2014-08-07T10:05:23Z
dc.date.available2014-08-07T10:05:23Z
dc.date.issued2009
dc.identifier.issn1309-9469
dc.identifier.urihttp://hdl.handle.net/11424/2185
dc.description.abstractFive years old girl, that has been followed as hereditary spherocytosis from the newborn period admitted to hospital for erythematous and violet-colored lesions. Physical examination revealed petechiae, purpura and ecchymoses on her body. She was evaluated and diagnosed as immune thrombocytopenic purpura. For many diseases heredity contributes to disease susceptibility and outcome. The molecular bases of hereditary spherocytosis have been unraveled but this is not valid for immune thrombocytopenic purpura. Genetic contributors in complex diseases such as immune thrombocytopenic purpura are new dimensions to studies on immune thrombocytopenic purpura. This is the first case, reported in literature with immune thrombocytopenic purpura and hereditary spherocytosis association.en_US
dc.language.isoenen_US
dc.publisherMarmara Medical Journalen_US
dc.subjectAssociation, child, comorbidity, hereditary spherocytosis, immune thrombocytopenic purpuraen_US
dc.titleThe association of immune thrombocytopenic purpura with hereditary spherocytosisen_US
dc.typeArticleen_US


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