Meckel Gruber Syndrome: A Case Report


Authors : ELBARAKA Yassine; AMMOR Younes. SAOUD karam; MAMOUNI Nisrine; ERRARHAY Sanaa; BOUCHIKHI Chahrazed; BANANI Abdelaziz

Volume/Issue : Volume 6 - 2021, Issue 1 - January

Google Scholar : http://bitly.ws/9nMw

Scribd : https://bit.ly/39zv5pj

Meckel Gruber syndrome is a uncommon poly malformative syndrome. It is an autosomal recessive disorder. The most common malformations found in Meckel syndrome are polycystic renal dysplasia, encephalocele, polydactyly, and hepatic fibrosis. Genetic progress in order to isolate the gene responsible for Meckel syndrome can help diagnosis, especially antenatal diagnosis. We report a case of Meckel syndrome discovered by ultrasound in labor.

Keywords : Meckel Syndrome, Renal Dysplasia, Polydactyly, Antenatal Diagnosis

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