A case of Roberts syndrome: its ultrasonographic characteristics and genetic diagnosis
Objective: Roberts syndrome is a very rare genetic disease, and it has an autosomal recessive inheritance pattern. It develops as a result of the mutation in ESCO2 gene located in the 8th chromosome. In our study, we aimed to present a case which was found to have Roberts syndrome coexistin...
| Main Authors: | , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Perinatal Medicine Foundation
2020-12-01
|
| Series: | Perinatal Journal |
| Online Access: | https://perinataljournal.com/Archive/Article/20200283009 |