Fig. 1From: Familial inheritance of the 3q29 microdeletion syndrome: case report and reviewFacial features of the proband and his affected mother. Note the similar broad nasal bridge seen in both the parent and proband (a). A closer look at the proband reveals periorbital puffiness and slightly downward slanting palpebral fissures (b). Profile views of the proband and his mother demonstrate similar ears with an overfolded helix (c-d)Back to article page