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...

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Detalles Bibliográficos
Autores principales: Traisrisilp, Kuntharee, Yanase, Yuri, Phirom, Krittaya, Tongsong, Theera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030570/
https://www.ncbi.nlm.nih.gov/pubmed/35453933
http://dx.doi.org/10.3390/diagnostics12040885

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030570/
https://www.ncbi.nlm.nih.gov/pubmed/35453933
http://dx.doi.org/10.3390/diagnostics12040885

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