产前超声诊断胎儿先天性多发性关节挛缩症1例

李诗慧,解丽梅

中国临床医学影像杂志 ›› 2018, Vol. 29 ›› Issue (4) : 304-304.

中国临床医学影像杂志 ›› 2018, Vol. 29 ›› Issue (4) : 304-304.
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产前超声诊断胎儿先天性多发性关节挛缩症1例

  • 李诗慧,解丽梅
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Prenatal ultrasonographic diagnosis of arthrogryposis multiplex congenita in fetuses: report of one case

  • LI Shi-hui, XIE Li-mei
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李诗慧,解丽梅. 产前超声诊断胎儿先天性多发性关节挛缩症1例[J]. 中国临床医学影像杂志. 2018, 29(4): 304-304
LI Shi-hui, XIE Li-mei. Prenatal ultrasonographic diagnosis of arthrogryposis multiplex congenita in fetuses: report of one case[J]. Journal of China Clinic Medical Imaging. 2018, 29(4): 304-304
中图分类号: R684    R714.5    R445.1   

参考文献

[1]Ekhilevitch N, Kurolap A, Oz-Levi D, et al. Expanding the MYBPC1 phenotypic spectrum: a novel homozygous mutation causes arthrogryposis multiplex congenita[J]. Clinical Genetics, 2016, 90(1): 84-89.
[2]张红彬,栗河舟,郭丽亚,等. 胎儿期多发性关节挛缩症的超声影像学特征[J]. 中国妇幼保健,2015,30(20):3498-3499.
[3]Leyser M, Fernandes A, Passos P, et al. Microcephaly and arthrogryposis multiplex congenita: the full-blown CNS spectrum in newborns with ZIKV infection[J]. J Neurol Sci, 2017, 372: 73-74.
[4]王继伟,皮小兰,刘燕娜,等. 超声诊断胎儿先天性多发性关节挛缩症1例[J]. 中国医学影像学杂志,2016,24(9):688.
[5]Feingold-Zadok M, Chitayat D, Chong K, et al. Mutations in the NEB gene cause fetal akinesia/arthrogryposis multiplex congenita[J]. Prenat Diagn, 2017, 37(2): 144-150.
[6]Kowalczyk B, Felus J. Treatment of foot deformities in arthrogryposis multiplex congenita[J]. JBJS Rev, 2015, 3(6): e4.
[7]Graydon AJ, Eastwood DM. Orthopaedic management of arthrogryposis multiplex congenital[J]. Eur Surg Orthop Traumatol, 2014, 22(4): 4627-4644.

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