Title: Meckel Gruber syndrome, A case report (3 cases)
Authors: Mohamed Saleh Abderrahmane
RAHMOUNE Mohammed
Chaara Hekmat
Jayi Sofia
Fdili Alaoui Fatima Zahra
Melhouf My Abdellilah
Volume: 5
Issue: 10
Pages: 1-5
Publication Date: 2021/10/28
Abstract:
: Meckel Gruber syndrome is a rare autosomal recessive poly malformative syndrome defined by occipital encephalocele, polydactyly and cystic renal dysplasia. Ultrasound is currently the best tool for antenatal screening of this lethal poly malformation and its confirmation is done by karyotype study. We report three cases of Meckel syndrome discovered by ultrasound.