Figure 1.

Facial aspects and specific malformations in patients with criptic subtelomeric anomalies. (a) Patient 3: note round face, low frontal hairline, hypertelorism and synophris; (b) Patient 4: note epicanthal folds, upslanting palpebral fissures and low-set ears; (c-d) Patient 5: note mild trigonochephaly and evolution of the phenotype at follow-up; (e-f) Patient 6: note plagiochephaly, palpebral ptosis and evolution of the phenotype at follow- up; (g-h-i) Patient 7: note macrotia and evolution of the phenotype at follow-up; (l-m-n-o) Patient 8: note severe hypertelorism, epicanthal folds and right external ear malformation and their evolution at follow-up; (p-q) Patient 9: note flat face, low-set ears and foot malformation; (r) Patient 10: note the coarse face.