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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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| Vydáno v: | J Ultrasound |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer International Publishing
2017
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| Témata: | |
| On-line přístup: | 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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