A down syndrome patient diagnosed with transient myeloproliferative disease after presenting with cutaneous findings
dc.contributor.author | Ceran, Burak | |
dc.contributor.author | Derme, Turan | |
dc.contributor.author | Erkan, Mehmet Orhan | |
dc.contributor.author | Sahin, Seda | |
dc.contributor.author | Gurlek Gokcebay, Dilek | |
dc.contributor.author | Cakir, Ufuk | |
dc.contributor.author | Tayman, Cuneyt | |
dc.date.accessioned | 2022-03-15T09:08:38Z | |
dc.date.available | 2022-03-15T09:08:38Z | |
dc.date.issued | 2021 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Transient myeloproliferative disease (TMD) is among the main hematologic problems seen in neonates with Down syndrome (DS). It is usually self-limiting and results in spontaneous remission within 3 to 6 months. Characteristic signs of TMD are leukocytosis, thrombocytopenia, anemia, hepatosplenomegaly, cutaneous nodules, and increased numbers of circulating blasts. In this article, we present a DS neonate without leukocytosis who was diagnosed as having TMD after a diffuse vesiculopapular eruption on the face, which is a different clinical presentation than other cases in the literature. Our aim is to emphasize the importance of early diagnosis and close multidisciplinary monitoring of these patients. | en_US |
dc.identifier.citation | Ceran, B., Derme, T., Erkan, M. O., Sahin, S., Gokcebay, D. G., Cakir, U., & Tayman, C. (2021). A down syndrome patient diagnosed with transient myeloproliferative disease after presenting with cutaneous findings. Annals of Medical Research, | en_US |
dc.identifier.uri | https://hdl.handle.net/11616/55601 | |
dc.language.iso | en | en_US |
dc.relation.ispartof | Annals of Medical Research | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.title | A down syndrome patient diagnosed with transient myeloproliferative disease after presenting with cutaneous findings | en_US |
dc.type | Article | en_US |