22q11.2 Deletion Syndrome / Di George / VCF
22q11.2 deletion syndrome is an "underdiagnosed" syndrome that occurs in 1:4000 births and 1:1000 fetuses, which major features includes: distinctive facial features, congenital heart disease (frequently conotruncal), velopharyngeal insufficiency or cleft palate, hypocalcemia, immune defic...
| Main Author: | |
|---|---|
| Format: | Online |
| Language: | English |
| Published: |
Facultad de Ciencias Exactas, Químicas y Naturales
2024
|
| Subjects: | |
| Online Access: | https://www.fceqyn.unam.edu.ar/recyt/index.php/recyt/article/view/789 |