{Reference Type}: Case Reports
{Title}: Meckel-Gruber Syndrome: A Case Who Lived for 5 Months.
{Author}: Aydin Ozturk P;Asena M;Katar S;Ozturk U;
{Journal}: Pediatr Neurosurg
{Volume}: 54
{Issue}: 4
{Year}: 2019
{Factor}: 1.165
{DOI}: 10.1159/000500766
{Abstract}: 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.