Meckel Gruber syndrome associated with anencephaly—an unusual reported case

Meckel–Gruber syndrome (MGS) is a rare and lethal ciliopathic disorder, with the incidence ranging between 1 in 13 000–400 000 live births. MGS is characterized by multisystem developmental malformations with the classical features of renal cystic dysplasia, occipital encephalocele and post-axial po...

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Detalles Bibliográficos
Autores principales: Yaqoubi, Houda Nasser Al, Fatema, Nishat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806412/
https://www.ncbi.nlm.nih.gov/pubmed/29479449
http://dx.doi.org/10.1093/omcr/omx092

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806412/
https://www.ncbi.nlm.nih.gov/pubmed/29479449
http://dx.doi.org/10.1093/omcr/omx092

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