Probable Moyamoya Syndrome in Association with Hemophilia A in an Infant.
作者信息
Saini Arushi Gahlot, Goswami Jyotindra Narayan, Suthar Renu, Sankhyan Naveen, Vyas Sameer, Singhi Pratibha
机构信息
Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Department of Radiodiagnosis, Post Graduate Institute of Medical Education and Research, Chandigarh, India.
出版信息
Indian J Pediatr. 2017 Feb;84(2):164-165. doi: 10.1007/s12098-016-2229-5. Epub 2016 Sep 15.
PMID:27638653
Abstract
摘要
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X-linked moyamoya syndrome associated with severe haemophilia A.与重度甲型血友病相关的X连锁烟雾病综合征
Haemophilia. 2016 Jan;22(1):e51-4. doi: 10.1111/hae.12806. Epub 2015 Sep 30.
2
Novel severe hemophilia A and moyamoya (SHAM) syndrome caused by Xq28 deletions encompassing F8 and BRCC3 genes.由包含F8和BRCC3基因的Xq28缺失引起的新型重度A型血友病和烟雾病（SHAM）综合征。
Blood. 2014 Jun 19;123(25):4002-4. doi: 10.1182/blood-2014-02-553685.
3
Life-threatening thrombosis complicating the management of hepatic hemorrhage: anticoagulant treatment in a newborn with hemophilia B.危及生命的血栓形成使肝出血的治疗复杂化：1例乙型血友病新生儿的抗凝治疗
J Pediatr Hematol Oncol. 2004 Apr;26(4):258-63. doi: 10.1097/00043426-200404000-00010.
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Moyamoya disease associated with hemophilia A. Case report.与甲型血友病相关的烟雾病。病例报告。
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5
Cerebral infarct associated with factor V Leiden mutation in a boy with hemophilia A.一名患有甲型血友病的男孩发生与凝血因子V莱顿突变相关的脑梗死。
Am J Hematol. 1997 Nov;56(3):189-90. doi: 10.1002/(sici)1096-8652(199711)56:3<189::aid-ajh11>3.0.co;2-6.
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