Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants.

TP63 基因突变和 LZTR1 基因变异的胎儿非免疫性胎儿水肿的自发消退.

• 发表时间: Aug 2021
• 来源期刊: Clin Case Rep
• DOI: 10.1002/ccr3.4624
• PMID: 34401172
• 文章类型: Case Reports
• 作者列表: Hurni Y,Marangoni M,Garofalo G,Cassart M,Tomasi L,Vandernoot I,Smits G,Gounongbé C

关键词: EEC syndrome; LZTR1 gene; TP63 gene; fetal medicine; hydrops fetalis

Abstract

In cases of fetal hydrops, searching for an etiology is essential to evaluate the fetal prognosis and propose the most appropriate management.

摘要

在胎儿水肿的情况下，寻找病因对于评估胎儿预后和提出最合适的治疗方法至关重要。