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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...
Tallennettuna:
| Julkaisussa: | Oxf Med Case Reports |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5806412/ https://ncbi.nlm.nih.gov/pubmed/29479449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omx092 |
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