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Meckel-Gruber syndrome: A rare and lethal anomaly with review of literature
Meckel-Gruber syndrome is a rare autosomal recessive lethal malformation characterized by typical manifestations of occipital encephalocele, bilateral polycystic kidneys and post axial polydactyly. The worldwide incidence varies from 1 in 13,250 to 1 in 140,000 live births. Highest incidence was rep...
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| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications & Media Pvt Ltd
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3783728/ https://ncbi.nlm.nih.gov/pubmed/24082939 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.117855 |
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