医学
产前诊断
儿科
磁共振成像
怀孕
先天性畸形
遗传性疾病
先天性疾病
常染色体隐性遗传
胎儿
产前超声
遗传咨询
多囊性肾病
先天性疾病
产科
血缘关系
超声波
超声科
外科
多囊肾
作者
Khouloud Moulehi,Imen Bannour,Chayma Rjiba,Salma Ben Youssef,Manel Kaabi,Mohamed Mallouli,Hafedh Touileb,Mohamed Mnasri,S. Bouguizène,Badra Bannour
标识
DOI:10.11604/pamj.2025.52.162.47620
摘要
Meckel-Gruber syndrome is a rare congenital disorder characterized by multiple malformations. It transmits via a recessive autosomal mode. It is characterized by an occipital encephalocele, polydactyly, and polycystic renal dysplasia. The diagnosis could be established via ultrasound. In fact, it is actually the key method for the early screening of this lethal malformation with at least two of its main characteristics. However, the diagnosis is confirmed by karyotype analysis. Herein, we present a case of Meckel-Gruber syndrome diagnosed in a fetus from a consanguineous marriage in a 40-year-old woman, gravida 2 para 1, with one previous healthy child. This pregnancy was terminated at 19 weeks of gestation. The diagnosis was made through prenatal ultrasound and magnetic resonance imaging (MRI). With later confirmation by fetal autopsy.
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