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Title: Meckel-Gruber syndrome. Author: Gazioğlu N, Vural M, Seçkin MS, Tüysüz B, Akpir E, Kuday C, Ilikkan B, Erginel A, Cenani A. Journal: Childs Nerv Syst; 1998 Mar; 14(3):142-5. PubMed ID: 9579873. Abstract: Meckel-Gruber syndrome is a congenital disorder characterized by occipital encephalocele, polydactyly and polycystic kidneys. This rare syndrome has been reported in the literature as incompatible with life. We present the case of a newborn afflicted with the clinical triad of Meckel-Gruber syndrome. Appropriate treatment instituted in our case led to a good early outcome.[Abstract] [Full Text] [Related] [New Search]