Hurler综合征
医学
移植
造血干细胞移植
造血细胞
儿科
内科学
疾病
重症监护医学
造血
干细胞
生物
遗传学
作者
Mieke Aldenhoven,Robert Wynn,Paul J. Orchard,Anne O’Meara,Paul Veys,Alain Fischer,Vassili Valayannopoulos,Bénédicte Neven,Attilio Rovelli,Vinod K. Prasad,Jakub Tolar,Heather Allewelt,Simon Jones,Rossella Parini,Marleen Renard,Victoria Bordon,Nico Wulffraat,Tom J. de Koning,Elsa Shapiro,Joanne Kurtzberg
出处
期刊:Blood
[Elsevier BV]
日期:2015-01-26
卷期号:125 (13): 2164-2172
被引量:309
标识
DOI:10.1182/blood-2014-11-608075
摘要
Key Points Patients with Hurler syndrome show significant residual disease burden despite HCT. Early referral for HCT, using noncarrier donors and regimens designed to achieve full-donor chimerism, offers the best long-term prognosis.
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