先天性疾病和羊水过多与疑似爱德华兹综合征

IF 0.7 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Fitra Afdanil, Kusika Saputra NP
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引用次数: 0

摘要

本研究的目的是识别和分析先天性疾病和羊水过多与疑似爱德华兹综合征。本研究采用的方法是一例43岁妊娠39-40周妊娠G4P3A0H3的患者。本研究结果表明,先天性畸形是固有的,并定义为结构,功能或代谢异常,由于畸形的内容物。2010年,先天性异常占新生儿死亡的10.5%。这些异常在本质上是先天性的,通常是独立发现的,但在一个条件下,多种异常可以同时出现。发现一个异常可以提供良好的预后,但发现几个异常可能会破坏婴儿的健康。在本研究中,我们报告了一个先天性异常的新生儿(肛门闭锁,小颌,双侧唇腭裂,低耳和摇脚)。没有病史、家族史和产科史,也没有体验性疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital Disorders and Polyhydramnios with Suspected Edwards Syndrome
The aim of this research is to identify and analyze congenital disorders and polyhydramnios with suspected Edwards syndrome. The method used in this study is a case report of a 43-year-old patient with a gravidity of G4P3A0H3 at 39-40 weeks of gestation. The results of this research indicate that congenital anomalies are inherent and defined as structural, functional, or metabolic abnormalities due to malformation of the contents. In 2010, congenital anomalies accounted for 10.5% of neonatal deaths. These anomalies are congenital in nature and are usually found independently, but multiple anomalies can be present together in a condition. Finding one anomaly can provide a favorable prognosis, but finding several anomalies can disrupt the baby's well-being. In the study, we report a neonate with congenital anomalies (anal atresia, micrognathia, bilateral cleft lip and palate, low-set ears, and rocker bottom foot). There is no history of illness, family and obstetric history, and no experiential disorders.
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来源期刊
International Journal of Migration Health and Social Care
International Journal of Migration Health and Social Care PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
1.30
自引率
0.00%
发文量
21
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