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Meckel-Gruber Syndrome: A Case Who Lived for 5 Months
Pinar Aydin Ozturk1, Muhammet Asena2, Salim Katar3
1Department of Neurosurgery, Health Science University Gazi Yasargil Education Research Hospital, Diyarbakir, Turkey, aydinpinar12@gmail.com.
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.
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