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FGA基因c.1368delC纯合框移突变致先天性无纤维蛋白原血症1例

何丽婷 潘家华

何丽婷, 潘家华. FGA基因c.1368delC纯合框移突变致先天性无纤维蛋白原血症1例[J]. 中华全科医学, 2023, 21(1): 172-175. doi: 10.16766/j.cnki.issn.1674-4152.002838
引用本文: 何丽婷, 潘家华. FGA基因c.1368delC纯合框移突变致先天性无纤维蛋白原血症1例[J]. 中华全科医学, 2023, 21(1): 172-175. doi: 10.16766/j.cnki.issn.1674-4152.002838
HE Li-ting, PAN Jia-hua. Congenital afibrinogenemia caused by homozygous frame-shift mutation of FGA gene c.1368delC: a case report and literature review[J]. Chinese Journal of General Practice, 2023, 21(1): 172-175. doi: 10.16766/j.cnki.issn.1674-4152.002838
Citation: HE Li-ting, PAN Jia-hua. Congenital afibrinogenemia caused by homozygous frame-shift mutation of FGA gene c.1368delC: a case report and literature review[J]. Chinese Journal of General Practice, 2023, 21(1): 172-175. doi: 10.16766/j.cnki.issn.1674-4152.002838

FGA基因c.1368delC纯合框移突变致先天性无纤维蛋白原血症1例

doi: 10.16766/j.cnki.issn.1674-4152.002838
基金项目: 

国家卫生健康委员会医药卫生科技发展项目 WA2020HK60

详细信息
    通讯作者:

    潘家华,E-mail:panjiahua1960@163.com

  • 中图分类号: R554  R446.7

Congenital afibrinogenemia caused by homozygous frame-shift mutation of FGA gene c.1368delC: a case report and literature review

  • 摘要: 先天性无纤维蛋白原血症主要表现为反复的出血包括脐部出血、青紫、鼻出血、牙龈出血、脾出血、肝出血、胃肠道或泌尿生殖道出血等。本案例患者出生后反复出血、反复低纤维蛋白原血症,经过先天性无纤维蛋白原血症基因筛查及家系验证提示患儿系FGA基因,核酸突变c.1368delC纯合框移变异,氨基酸突变p.T457Rfs*27。其父母均携带该位点杂合框移变异。后患儿出现肺出血,但无相关临床症状与体征,经过布地奈德福莫特罗粉吸入剂早晚两次雾化吸入治疗1个月后,肺部出血病灶明显吸收。

     

  • 图  1  患者全腹部CT图

    Figure  1.  Sanger sequencing peak map of proband and their parents in FGA gene c.1368delC whole abdominal CT images of patients

    图  2  患者肺部CT三维重建图

    Figure  2.  CT 3D reconstruction of the patient' s lung

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    WANG Y, ZHANG Z H, WANG L H, et al. A pedigree of congenital dysfibrinogenemia[J]. Chinese Journal of Internal Medicine, 2020, 59(4): 311-312, 313. doi: 10.3760/cma.j.cn112138-20190730-00525
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    [6] SAES J L, LAROS-VAN G B A P, COPPENS M, et al. Pregnancy outcome in afibrinogenemia: are we giving enough fibrinogen concentrate? A case series[J]. Res Pract Thromb Hae, 2020, 4(2): 343-346. doi: 10.1002/rth2.12300
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    [8] 苏正仙, 毕晓洁, 金先富, 等. FGA基因c. 104G>A杂合突变导致的先天性低纤维蛋白原血症家系的基因分析[J]. 浙江医学, 2019, 41(6): 594-596.

    SU Z X, BI X J, JIN X F, et al. FGA gene c. 104 g > A heterozygous mutations can lead to congenital low fibrinogen concentration family genetic analysis[J]. Zhejiang Medical Journal, 2019, 41(6): 594-596.
    [9] LISSITCHKOV T, MADAN B, DJAMBAS K C, et al. Fibrinogen concentrate for treatment of bleeding and surgical prophylaxis in congenital fibrinogen deficiency patients[J]. J Thromb Haemost, 2020, 18(4): 815-824. doi: 10.1111/jth.14727
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    [11] 罗美玲, 闫婕, 林发全, 等. 二例无症状遗传性异常纤维蛋白原血症患者的手术治疗[J]. 中华血液学杂志, 2017, 38(9): 797-798.

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出版历程
  • 收稿日期:  2022-01-30
  • 网络出版日期:  2023-04-07

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