Prenatal Sonographic Features of Ring Chromosome 15: A Case Report and Literature Review
Ring chromosome 15, a rare genetic disease, is very rarely prenatally diagnosed. We present a unique case of fetal ring chromosome 15 with ultrasound findings at 32 weeks of gestation including congenital diaphragmatic hernia, hypoplasia of the aorta with persistent left SVC, growth restriction, clu...
Guardado en:
| Autores principales: | , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
MDPI AG
2022-04-01
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| Colección: | Diagnostics |
| Materias: | |
| Acceso en línea: | https://www.mdpi.com/2075-4418/12/4/885 |
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