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Meckel–Gruber syndrome: ultrasonographic and fetal autopsy correlation

Meckel–Gruber syndrome (MGS) is a rare autosomal recessive disorder which is characterized by a classic triad of occipital encephalocele, polycystic kidneys and postaxial polydactyly. We describe a case of classic MGS, diagnosed on ultrasonography and genetic analysis, with subsequent confirmation a...

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Detalhes bibliográficos
Publicado no:J Ultrasound
Main Authors: Khurana, Shruti, Saini, Vikram, Wadhwa, Vibhor, Kaur, Harveen
Formato: Artigo
Idioma:Inglês
Publicado em: Springer International Publishing 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5440330/
https://ncbi.nlm.nih.gov/pubmed/28593008
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s40477-016-0231-4
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