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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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Bibliografiske detaljer
Main Authors: Myageri, Aneel, Grampurohit, Vandana, Rao, Ravikala
Format: Artigo
Sprog:Inglês
Udgivet: Medknow Publications & Media Pvt Ltd 2013
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3894002/
https://ncbi.nlm.nih.gov/pubmed/24479060
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2249-4863.109971
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