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Meckel Gruber Syndrome: Report of Two Cases with Review of Literature

Meckel Gruber syndrome (MKS) is a lethal, autosomal, recessive, multisystemic disorder, associated with mutations affecting ciliogenesis. Since the time it was first reported; only 200 cases have been reported. From January 2004 to December 2010, we evaluated 268 fetal autopsies in our institute, in...

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Detalles Bibliográficos
Autores principales:	Myageri, Aneel, Grampurohit, Vandana, Rao, Ravikala
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2013
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894002/ https://www.ncbi.nlm.nih.gov/pubmed/24479060 http://dx.doi.org/10.4103/2249-4863.109971

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