Gazioğlu N, Vural M, Seçkin M S, Tüysüz B, Akpir E, Kuday C, Ilikkan B, Erginel A, Cenani A
Department of Neurosurgery, Istanbul University, Cerrahpaşa Faculty of Medicine, Turkey.
Childs Nerv Syst. 1998 Mar;14(3):142-5. doi: 10.1007/s003810050198.
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.
梅克尔-格鲁伯综合征是一种先天性疾病，其特征为枕部脑膨出、多指（趾）畸形和多囊肾。这种罕见的综合征在文献中被报道为与生命不相容。我们报告了一例患有梅克尔-格鲁伯综合征临床三联征的新生儿病例。我们对该病例采取的适当治疗取得了良好的早期效果。
