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Multiple Congenital Anomalies in a Patient with Interstitial 6q26 Deletion
We report a preterm male neonate presenting with a lumbosacral meningomyelocele, type II Arnold Chiari malformation, hypoplasia of the aortic arch, bicuspid aortic valve, ventricular septal defect, secundum atrial septal defect, multicystic dysplastic kidney, and hydronephrosis. Analysis with whole...
Tallennettuna:
| Julkaisussa: | Mol Syndromol |
|---|---|
| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
S. Karger AG
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6997795/ https://ncbi.nlm.nih.gov/pubmed/32021599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000503698 |
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