Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Trevor B. Cabrera"'
Autor:
Trevor B. Cabrera, Allison L. Speer, Matthew R. Greives, Donna A. Goff, Neethu M. Menon, Eric W. Reynolds
Publikováno v:
American Journal of Perinatology Reports, Vol 10, Iss 04, Pp e390-e394 (2020)
We present a case of a neonate born with kaposiform hemangioendothelioma (KHE), complicated by Kasabach-Merritt phenomenon (KMP) and other serious conditions, who was successfully treated with sirolimus. In addition to complications from thrombocytop
Externí odkaz:
https://doaj.org/article/9745bb35c32d40f594ac59930df68a5f
Autor:
Donna A. Goff, Trevor B. Cabrera, Matthew R. Greives, Allison L. Speer, Eric W. Reynolds, Neethu M. Menon
Publikováno v:
AJP Reports
American Journal of Perinatology Reports, Vol 10, Iss 04, Pp e390-e394 (2020)
American Journal of Perinatology Reports, Vol 10, Iss 04, Pp e390-e394 (2020)
We present a case of a neonate born with kaposiform hemangioendothelioma (KHE), complicated by Kasabach-Merritt phenomenon (KMP) and other serious conditions, who was successfully treated with sirolimus. In addition to complications from thrombocytop
Autor:
Wei Wang, Branko Cuglievan, John M. Slopis, Sireesha Yedururi, Trevor B. Cabrera, Michael Rytting, Raphael E Steiner
Publikováno v:
Journal of pediatric hematology/oncology. 43(4)
Neurofibromatosis Type 1 (NF1) is a genetic disorder with an incidence of 1 in 2600 to 3000 individuals. It is a clinical diagnosis characterized by cafe-au-lait macules, neurofibromas, and axillary and/or groin freckling. Because of genetic mutation