Fetal edema caused by PIEZO1 mutation: a case report

doi:10.3877/cma.j.issn.2095-3259.2021.02.011

Chinese Journal of Obstetric Emergency(Electronic Edition) ›› 2021, Vol. 10 ›› Issue (02): 113-115. doi: 10.3877/cma.j.issn.2095-3259.2021.02.011

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Fetal edema caused by PIEZO1 mutation: a case report

Zhenyu Zhang¹, Huina Liu¹(), Wenjing Yuan¹

Received:2020-12-09 Online:2021-05-18 Published:2021-07-14
Contact: Huina Liu

Abstract

Zhenyu Zhang, Huina Liu, Wenjing Yuan. Fetal edema caused by PIEZO1 mutation: a case report[J]. Chinese Journal of Obstetric Emergency(Electronic Edition), 2021, 10(02): 113-115.

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References 10

[1]	杨芳，徐彩玲．胎儿水肿病因学分析及诊治进展[J]．中华产科急救电子杂志，2018，7(1)：24-29.
[2]	Sparks TN, Thao K, Lianoglou BR, et al. Nonimmune hydrops fetalis: identifying the underlying genetic etiology[J]. Genet Med，2019, 21(6)：1339-1344.
[3]	Norton ME, Chauhan SP, Dashe JS. Society for Maternal-Fetal Medicine (SMFM). Clinical Guideline #7: nonimmune hydrops fetalis[J]. AM J Obstet Gynecol, 2015, 212(2)：127-139.
[4]	麻希洋，吴庆华. 非免疫性胎儿水肿的遗传学研究进展[J]. 中华医学遗学杂志，2018, 35(1)：125-128.
[5]	Gordon K, Spiden SL, Connell FC, et al. FLT4/VEGFR3 and Milroy disease: novel mutations, a review of published variants and database update[J]. Hum Mutat, 2013, 34(1)：23-31.
[6]	Fotiou E, Martin-Almedina S, Simpson MA, et al. Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis[J]. Nat Commun, 2015, 6：8085.
[7]	Guo W, Lai Y, Yan Z, et al. Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations[J]. Hum Mutat, 2020, 41(2)：432-448.
[8]	殷荣，杨琳，胡黎园，等. 基于全外显子组测序对病因不明致死性胎儿水肿遗传学病因的初步分析[J]．中国循证儿科杂志，2017，12(4): 278-283.
[9]	Stosic M, Levy B, Wapner R. The use of chromosomal microarray analysis in prenatal diagnosis[J]. Obstet Gynecol Clin North Am, 2018，45(1)：55-68.
[10]	Brown TL, Meloche TM. Exome sequencing a review of new strategies for rare genomic disease research[J]. Genomics, 2016，108(3-4): 109-114.

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