Prenatal Ultrasound Signs of Cornelia de Lange Syndrome in Monochorionic Twins: Case Study

• Autori principali: Nodira M. Normuradova (Autore), Odil A. Khujakulov (Autore), Mahliyo Sh. Ergasheva (Autore), Eshdavlat R. Ollanazarov (Autore), Bekhruz B. Majidov (Autore)
• Natura: Libro
• Pubblicazione: "Paediatrician" Publishers LLC, 2022-03-01T00:00:00Z.
• Soggetti: article
• Accesso online: Connect to this object online.

Background. Cornelia de Lange syndrome is rare genetic disease manifested by short stature, limb abnormalities, craniofacial dysmorphies, and developmental delay. Syndrome prenatal detection is crucial during ultrasound diagnosis.Clinical case description. Growth delay of both children (body weight...