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...
| Autori principali: | , , , |
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| Natura: | Articolo |
| Lingua: | English |
| Pubblicazione: |
MDPI AG
2022-04-01
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| Serie: | Diagnostics |
| Soggetti: | |
| Accesso online: | https://www.mdpi.com/2075-4418/12/4/885 |