| Literature DB >> 9579873 |
N Gazioğlu1, M Vural, M S Seçkin, B Tüysüz, E Akpir, C Kuday, B Ilikkan, A Erginel, A Cenani.
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.Entities:
Mesh:
Year: 1998 PMID: 9579873 DOI: 10.1007/s003810050198
Source DB: PubMed Journal: Childs Nerv Syst ISSN: 0256-7040 Impact factor: 1.475