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A rare variation of hydranencephaly: case report
Hydranencephaly is a rare congenital abnormality characterized by the absence and replacement of the cerebral hemispheres with cerebrospinal fluid. Here, we present an ultrasonographic diagnosis of a case of a rare variant of fetal hydranencephaly at 38 weeks of gestation. Obstetric sonography revea...
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
F1000Research
2014
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3945765/ https://ncbi.nlm.nih.gov/pubmed/24627761 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.1-22.v3 |
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