Case Report

8q22.2q22.3 Microdeletion Syndrome Associated with Hearing Loss and Intractable Epilepsy

Figure 1

Microdeletion syndrome involving 8q22.2q22.3. Female patient at the age of 10 years with microcephaly, triangular face, arched eyebrows, blepharophimosis, bilateral epicanthic fold, oblique palpebral fissures, midface hypoplasia, nostrils hypoplasia, short philtrum, thin upper lip, and down-turned corners of the mouth.