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| Prenatal ultrasonographic diagnosis of arthrogryposis multiplex congenita in fetuses: report of one case |
| LI Shi-hui, XIE Li-mei |
| Department of Ultrasonography, Shengjing Hospital of China Medical University, Shenyang 110004, China |
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[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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