Karner Eva, Krepler Lara, Pateisky Petra, Grill Agnes, Dremsek Paul, Yerlikaya-Schatten Guelen, Springer Stephanie
Department of Obstetrics and Gynecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Spitalgasse 23, 1090 Vienna, Austria.
Department of Pediatrics and Adolescent Medicine, Division of Neonatology, Intensive Care Medicine and Neuropediatrics, Medical University of Vienna, Spitalgasse 23, 1090 Vienna, Austria.
Life (Basel). 2025 Aug 1;15(8):1215. doi: 10.3390/life15081215.
Hypoplastic or absent fetal nasal bone (NB) is a significant soft marker in the risk assessment for aneuploidies. This study aimed to evaluate prenatal findings and perinatal outcomes in fetuses with absent or hypoplastic NB managed at our center. This retrospective analysis was conducted at the Department of Obstetrics at the Medical University of Vienna and including all cases with an absent or hypoplastic fetal NB between 2004 and 2022. Clinical data were extracted and analyzed using descriptive statistics. A total of 149 cases were included. Of these, 51% had chromosomal abnormalities, with trisomy 21 present in 30.9%. Malformations were identified in 55% of cases, most commonly congenital heart defects (34.9%) and facial dysmorphism (28.9%). Eighteen fetuses (12.1%) had structural anomalies without genetic disorders. In 32.9% (n = 49), the NB anomaly was isolated. Our findings show that only half of the cases had chromosomal abnormalities, and over half of the pregnancies resulted in live births with generally favorable perinatal outcomes. However, the presence of additional ultrasound abnormalities significantly increased the risk of adverse outcomes. Therefore, detection of a fetal NB anomaly should prompt comprehensive ultrasound evaluation and genetic testing.
胎儿鼻骨发育不全或缺失是评估非整倍体风险的一项重要软指标。本研究旨在评估在我们中心接受治疗的鼻骨缺失或发育不全胎儿的产前检查结果及围产期结局。这项回顾性分析在维也纳医科大学妇产科进行,纳入了2004年至2022年间所有鼻骨缺失或发育不全的病例。提取临床数据并采用描述性统计方法进行分析。共纳入149例病例。其中,51%存在染色体异常,21三体占30.9%。55%的病例发现有畸形,最常见的是先天性心脏病(34.9%)和面部畸形(28.9%)。18例胎儿(12.1%)有结构异常但无遗传疾病。32.9%(n = 49)的病例鼻骨异常为孤立性。我们的研究结果表明,只有一半的病例存在染色体异常,超过一半的妊娠以活产告终,围产期结局总体良好。然而,额外超声异常的存在显著增加了不良结局的风险。因此,检测到胎儿鼻骨异常应促使进行全面的超声评估和基因检测。