Fig. 1
From: Incidental finding of APC deletion in a child: double trouble or double chance? – a case report
Photograph of the patient at 2 years old. Minor facial anomalies reminiscent of 22q11.2DS are notable, including bitemporal constriction, low-set ears, sparse eyebrows, short palpebral fissures, bilateral epicanthic folds, depressed nasal bridge, tubular nose and mild hypoplastic alae nasi