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.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 |
http://hdl.handle.net/11616/55601 |
|
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.language.iso |
eng |
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 |
dc.relation.journal |
Annals of Medical Research |
en_US |
dc.contributor.department |
İnönü Üniversitesi |
en_US |