%0 Case Reports
%T Meckel-Gruber Syndrome: A Case Who Lived for 5 Months.
%A Aydin Ozturk P
%A Asena M
%A Katar S
%A Ozturk U
%J Pediatr Neurosurg
%V 54
%N 4
%D 2019
%M 31261150
%F 1.165
%R 10.1159/000500766
%X The Meckel-Gruber syndrome is a rare, congenital, and lethal malformation characterized by typical manifestations such as encephalocele, polycystic kidneys, and polydactyly. Herein, we present a case of a patient with the typical triad as well as facial, ocular, liver, and genital abnormalities who lived for almost 5 months.