Table 3 Findings in and indication for prenatally diagnosed patients
From: Clinical characterization of 72 patients with del(22)(q11.2q11.2) from different ethnic backgrounds
Country of origin | Indication for prenatal study | Sonographic findings | Other data of interest |
|---|---|---|---|
Cuba | Mother carrier of del(22) | Choledochal cysts and bilateral renal pyelectasis | Mother with dysmorphic features, without heart disease |
Cuba | Mother carrier of del(22) | Right aortic arch and thymic hypoplasia | Mother with dysmorphic features and learning disability |
India | Mother carrier of del(22) | Cardiac anomaly with thymic aplasia | Mother with 22q11.2DS phenotype |
Germany | Father carrier of del(22) | Not reported | Father with mental disorders and DGS phenotype |
India | Malformation detected by ultrasound | Multiple congenital anomalies. Cardiovascular malformation | |
Germany | Malformation detected by ultrasound | VSD, pulmonary valve stenosis, right aortic arch, riding aorta | |
Germany | Malformation detected by ultrasound | VSD + interrupted aortic arch | |
Germany | Malformation detected by ultrasound | Renal agenesis |