[FGA gene variation causing congenital dysfibrinogenemia with recurrent arteriovenous thrombosis]
Zhonghua Er Ke Za Zhi
.
2020 Mar 2;58(3):236-238.
doi: 10.3760/cma.j.issn.0578-1310.2020.03.016.
[Article in Chinese]
Authors
Y X He
1
,
J Yin
2
,
T T Liu
3
,
H M Gao
4
,
R Zhang
1
,
J F Yao
1
,
X Y Liu
2
,
X L Jia
4
,
X L Li
3
,
S L Li
3
,
R H Wu
1
Affiliations
1
Hematology Oncology Center, Beijing Children's Hospital, Capital Medical University, Beijing 100045, China.
2
Department of Respiratory Diseases, Beijing Children's Hospital, Capital Medical University,Beijing 100045, China.
3
Department of Emergency Surgery, Beijing Children's Hospital, CapitalmedicalUniversity, Beijing 100045, China.
4
Department of Critical Care Medicine, Capital Medical University, Beijing Children's Hospital, Beijing 100045, China.
PMID:
32135598
DOI:
10.3760/cma.j.issn.0578-1310.2020.03.016
Abstract
1例主诉为"间断腹痛、呕吐2个月余,加重3 d"的患儿就诊于北京儿童医院血液科,经过相关化验及基因测序检查,最终诊断为异常纤维蛋白原血症。以反复动、静脉血栓形成的异常纤维蛋白原血症临床罕见。.
MeSH terms
Afibrinogenemia* / congenital
Afibrinogenemia* / genetics
Fibrinogen / genetics*
Genetic Variation
Humans
Thrombosis* / genetics
Substances
Fibrinogen