Figure 1From: Concomitant deletion of chromosome 16p13.11 and triplication of chromosome 19p13.3 in a child with developmental disorders, intellectual disability, and epilepsy Patient at the age of 13Â years old. Note long coarse face, flat occiput, brachycephaly, hypertelorism, shortened palpebral fissures, broad nasal bridge and short nose, long philtrum, full prominent everted lower lips, open mouth, low set ears, maxillary hypoplasia.Back to article page